Allele Registry

Canonical Allele Identifier: PA2828036939

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV000498690

RCV003766796

ClinVar Variation:

432305

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341856.1:p.Gly83Ala	CA373291969 NM_001354927.2:c.248G>C