Canonical Allele Identifier: PA2499228426
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1224414
ClinVar RCV Id: RCV001597481
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp435Val
CA404885597
NM_000095.3:c.1304A>T