Canonical Allele Identifier: PA2741808914
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2881711
ClinVar RCV Id: RCV003708243
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Trp344Ser
CA9316557
NM_000095.3:c.1031G>C