Allele Registry

Canonical Allele Identifier: PA2828037007

Gene: VCP HGNC NCBI

ClinVar Variation Id: 280123

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341856.1:p.Arg114Cys	CA5039453 NM_001354927.2:c.340C>T