Allele Registry

Canonical Allele Identifier: PA658662945

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV000534353

RCV001579523

RCV002350262

RCV004537963

ClinVar Variation:

464105

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Asn401Ser	CA5039291 NM_007126.5:c.1202A>G