Allele Registry

Canonical Allele Identifier: PA658819016

Gene: VCP HGNC NCBI

ClinVar Allele:

524559

ClinVar RCV:

RCV000639654

RCV000993545

RCV001535609

ClinVar Variation:

532761

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Ala160Pro	CA373289512 NM_007126.5:c.478G>C