ClinVar Variation ID
ID clinvar_variation_id
DatatypeNot PIIidentifierDraft
This record is a draft: it has not been reviewed yet and may be incomplete or wrong. Do not rely on it for compliance decisions. Help improve it (see CONTRIBUTING.md).
Number of a variation record in ClinVar, the NCBI archive of reports on how human genetic variants relate to health conditions. The same record has an accession made of VCV and the number padded to nine digits, as in VCV000012345 for Variation ID 12345.
- Categories
- Medical/pharma identifiers, Scientific
- Countries
- Global (not tied to a country)
- Languages
- Common to most languages
- Bioregistry
clinvar.variation- Wikidata
- P1929
- Quality
- 85/100 · missing: translation, detector coverage
- Metacrafter rules
- no detection rule yet
- Supported by tools
- no tool record lists this type yet
Regular expression
^\d+$Python re syntax.
Examples
| Value | Description |
|---|---|
| 12345 | NM_001065.4(TNFRSF1A):c.295T>A (p.Cys99Ser); Bioregistry example |
| 7105 | CFTR p.Phe508del; example of Wikidata property P1929 |
| 13961 | BRAF V600E; example of Wikidata property P1929 |
| VCV000012345 invalid | VCV accession of the same record, not the Variation ID |
Sources
- doc: https://www.ncbi.nlm.nih.gov/clinvar/
- other: https://bioregistry.io/registry/clinvar.variation
- wikidata: https://www.wikidata.org/wiki/Property:P1929
Use this record
- Page URL:
http://registry.apicrafter.io/datatype/clinvar_variation_id - JSON: API v1 · legacy shape (used by metacrafter) · Markdown (for LLMs)
- Improve it: edit
data/datatypes/any/medical/clinvar_variation_id.yamlon GitHub