Allele Registry

Canonical Allele Identifier: PA213391

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV000202492

RCV001853259

ClinVar Variation:

218306

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Gly97Glu	CA213389 NM_007126.5:c.290G>A