Canonical Allele Identifier: PA2573061250
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 1332846
ClinVar RCV Id: RCV001806420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Cys328Phe
CA404890434
NM_000095.3:c.983G>T