Canonical Allele Identifier: PA645471469
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 328615
ClinVar RCV Id: RCV000320583 RCV000375163 RCV002521199 RCV003897750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Asp530Glu
CA9316351
NM_000095.3:c.1590C>A
CA404883017
NM_000095.3:c.1590C>G