Allele Registry

Canonical Allele Identifier: PA2828037552

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV000008991

RCV001172005

ClinVar Variation:

8470

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341857.1:p.Ala187Glu	CA254400 NM_001354928.2:c.560C>A