Canonical Allele Identifier: PA2741808973
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2579388
ClinVar RCV Id: RCV003327823
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp509Gly
CA404883555
NM_000095.3:c.1526A>G