Allele Registry

Canonical Allele Identifier: PA2573253802

Gene: VCP HGNC NCBI

ClinVar RCV:

RCV001949225

ClinVar Variation:

1457380

HGVS (amino-acid)	Matching Registered Transcripts
NP_009057.1:p.Arg155Ser	CA373289661 NM_007126.5:c.463C>A