Allele Registry

Canonical Allele Identifier: PA112063

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV000023065

ClinVar Variation:

30152

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Arg159Gly	CA259748 NM_007126.5:c.475C>G