Canonical Allele Identifier: PA100690
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 449473
ClinVar RCV Id: RCV000520014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Gly501Asp
CA404883780
NM_000095.3:c.1502G>A