Canonical Allele Identifier: PA2828037027
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 218305
ClinVar RCV Id: RCV000202444 RCV002229147 RCV002345722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341856.1:p.Glu140Lys
CA213386
NM_001354927.2:c.418G>A