Canonical Allele Identifier: PA645508625
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 280123
ClinVar RCV Id: RCV000333881 RCV001095425 RCV002229732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Arg159Cys
CA5039453
NM_007126.5:c.475C>T