Canonical Allele Identifier: PA2499228434
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1067222
ClinVar RCV Id: RCV001378429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asn489Lys
CA404884222
NM_000095.3:c.1467C>G
CA404884223
NM_000095.3:c.1467C>A