Canonical Allele Identifier: PA100545
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 9195
ClinVar RCV Id: RCV000009773 RCV003555993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Cys348Arg
CA254703
NM_000095.3:c.1042T>C