Canonical Allele Identifier: PA645508612
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 284302
ClinVar RCV Id: RCV000639655 RCV000390549 RCV001168987 RCV001252623 RCV001642885 RCV002418113 RCV004543043 RCV001168490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Ile27Val
CA5039558
NM_007126.5:c.79A>G