Allele Registry

Canonical Allele Identifier: PA112083

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV000008994

RCV000023064

RCV000516636

RCV000555373

RCV002496309

ClinVar Variation:

8473

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Arg191Gln	CA254406 NM_007126.5:c.572G>A