Allele Registry

Canonical Allele Identifier: PA2828037034

Gene: VCP HGNC NCBI

ClinVar Allele:

23512

ClinVar RCV:

RCV000008994

RCV000023064

RCV000516636

RCV000555373

RCV002496309

ClinVar Variation:

8473

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341856.1:p.Arg146Gln	CA254406 NM_001354927.2:c.437G>A