Canonical Allele Identifier: PA100621
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 9184
ClinVar RCV Id: RCV000009762 RCV002247283 RCV002512949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Cys468Tyr
CA254701
NM_000095.3:c.1403G>A