Canonical Allele Identifier: PA2828037475
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 280123
ClinVar RCV Id: RCV000333881 RCV001095425 RCV002229732
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Arg114Cys
CA5039453
NM_001354928.2:c.340C>T