Canonical Allele Identifier: PA2828037372
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 8471
ClinVar RCV Id: RCV000008992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Arg50Gly
CA254402
NM_001354928.2:c.148C>G