Allele Registry

Canonical Allele Identifier: PA2828036985

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV000008990

RCV000372207

RCV000685660

RCV001095424

ClinVar Variation:

8469

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341856.1:p.Arg110Cys	CA254398 NM_001354927.2:c.328C>T