Allele Registry

Canonical Allele Identifier: PA277491

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV000196145

RCV000494556

RCV002229498

ClinVar Variation:

217028

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Arg155Gly	CA277489 NM_007126.5:c.463C>G