Canonical Allele Identifier: PA2741808948
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2709843
ClinVar RCV Id: RCV003550146
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp458Gly
CA404884845
NM_000095.3:c.1373A>G