Allele Registry

Canonical Allele Identifier: PA112048

Gene: VCP HGNC NCBI

ClinVar Allele:

23511

ClinVar RCV:

RCV000008993

RCV001387337

RCV003137504

ClinVar Variation:

8472

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Arg155Pro	CA254404 NM_007126.5:c.464G>C