Canonical Allele Identifier: PA2741808964
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2841386
ClinVar RCV Id: RCV003718978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Cys484Phe
CA404884293
NM_000095.3:c.1451G>T