Canonical Allele Identifier: PA2573253828
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 1359439
ClinVar RCV Id: RCV001864719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Ile590Val
CA373276541
NM_007126.5:c.1768A>G