Canonical Allele Identifier: PA645471462
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 9192
ClinVar RCV Id: RCV000009770
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp472_Asp473dup