Canonical Allele Identifier: PA112083
Gene: VCP HGNC NCBI

Linked Data

ClinVar Variation Id: 8473
ClinVar RCV Id: RCV000008994 RCV000023064 RCV000555373 RCV000516636 RCV002496309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009057.1:p.Arg191Gln
CA254406
NM_007126.5:c.572G>A