Allele Registry

Canonical Allele Identifier: PA1139721874

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV001271083

ClinVar Variation:

989439

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Arg159Ser	CA373289529 NM_007126.5:c.475C>A