Allele Registry

Canonical Allele Identifier: PA2828036989

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV001949225

ClinVar Variation:

1457380

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341856.1:p.Arg110Ser	CA373289661 NM_001354927.2:c.328C>A