Canonical Allele Identifier: PA658662932
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 449554
ClinVar RCV Id: RCV000520021 RCV002231635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Arg93His
CA5039527
NM_007126.5:c.278G>A