Canonical Allele Identifier: PA2828037209
Gene: VCP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341856.1:p.Ile545Val
CA373276541
NM_001354927.2:c.1633A>G