Canonical Allele Identifier: PA213391
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 218306
ClinVar RCV Id: RCV000202492 RCV001853259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Gly97Glu
CA213389
NM_007126.5:c.290G>A