Canonical Allele Identifier: PA2828036894
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 218306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341856.1:p.Gly52Glu
CA213389
NM_001354927.2:c.155G>A