Allele Registry

Canonical Allele Identifier: PA2828037033

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV001095426

RCV003769035

ClinVar Variation:

873223

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341856.1:p.Arg146Pro	CA373288667 NM_001354927.2:c.437G>C