Allele Registry

Canonical Allele Identifier: PA2828037480

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV001271083

ClinVar Variation:

989439

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341857.1:p.Arg114Ser	CA373289529 NM_001354928.2:c.340C>A