Canonical Allele Identifier: PA2828037459
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 217028
ClinVar RCV Id: RCV000196145 RCV000494556 RCV002229498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Arg110Gly
CA277489
NM_001354928.2:c.328C>G