Canonical Allele Identifier: PA2828037462
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 8469
ClinVar RCV Id: RCV000008990 RCV000372207 RCV000685660 RCV001095424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Arg110Cys
CA254398
NM_001354928.2:c.328C>T