Canonical Allele Identifier: PA2573162347
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1498565
ClinVar RCV Id: RCV001999275
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Arg481Trp
CA9316422
NM_000095.3:c.1441C>T