Canonical Allele Identifier: PA112063
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_009057.1:p.Arg159Gly
CA259748
NM_007126.5:c.475C>G