Canonical Allele Identifier: PA100449
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 9191
ClinVar RCV Id: RCV000009769
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp473Gly
CA120169
NM_000095.3:c.1418A>G