ASassyro
ClinVar

Read one ClinVar record

Read one ClinVar variant by its VCV accession (or VariationID, or an RCV accession): its aggregate germline classification with review status and date last evaluated, somatic clinical impact and oncogenicity, every condition submitted, condition identifiers (MONDO, MedGen, OMIM, Orphanet), locations on each assembly, dbSNP and RCV accessions. Cite it by VCV accession and date last evaluated.

get/v1/sources/clinvar/records/{recordId}

Request

  • Base URL
    https://api.assyro.com
  • Auth
    none declared

Path parameters

recordIdstring required

The record id, as a search returned it (the read argument id).

Response

The record and its text.

versionunknown required
textstring nullable required
truncatedboolean required

Changes

No recorded changes to this operation across all 1 revision of this API.