Canonical Allele Identifier: PA277491
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 217028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Arg155Gly
CA277489
NM_007126.5:c.463C>G