Allele Registry

Canonical Allele Identifier: PA2828037460

Gene: VCP HGNC NCBI

ClinVar Allele:

23511

ClinVar RCV:

RCV000008993

RCV001387337

RCV003137504

ClinVar Variation:

8472

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341857.1:p.Arg110Pro	CA254404 NM_001354928.2:c.329G>C