Allele Registry

Canonical Allele Identifier: PA1139721882

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV001095426

RCV003769035

ClinVar Variation:

873223

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Arg191Pro	CA373288667 NM_007126.5:c.572G>C