Canonical Allele Identifier: PA2828036864
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1010487
ClinVar RCV Id: RCV001308126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341856.1:p.Arg44Trp
CA373293559
NM_001354927.2:c.130C>T