Canonical Allele Identifier: PA2828037478
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 30152
ClinVar RCV Id: RCV000023065
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Arg114Gly
CA259748
NM_001354928.2:c.340C>G