Canonical Allele Identifier: PA2825066456
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 3147931
ClinVar RCV Id: RCV004437764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Arg445Pro
CA9316435
NM_000095.3:c.1334G>C