Canonical Allele Identifier: PA1139698576
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 843498
ClinVar RCV Id: RCV001046138
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp548His
CA404882363
NM_000095.3:c.1642G>C