Canonical Allele Identifier: PA2828037319
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 2659168
ClinVar RCV Id: RCV003425656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341857.1:p.Thr11Ala
CA373294389
NM_001354928.2:c.31A>G