Allele Registry

Canonical Allele Identifier: PA645508618

Gene: VCP HGNC NCBI

ClinVar Allele:

425845

ClinVar RCV:

RCV000498690

RCV003766796

ClinVar Variation:

432305

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Gly128Ala	CA373291969 NM_007126.5:c.383G>C