Canonical Allele Identifier: PA2828037380
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 218306
ClinVar RCV Id: RCV000202492 RCV001853259
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Gly52Glu
CA213389
NM_001354928.2:c.155G>A