Allele Registry

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Canonical Allele Identifier: PA2827926573

Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 566162

ClinVar RCV Id: RCV000685906 RCV001018482 RCV002298738

ClinVar Variation Id: 1047144

ClinVar RCV Id: RCV001351817 RCV002377495 RCV002486456 RCV004005245

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341652.1:p.Gly30Arg	CA70042258 NM_001354723.2:c.88G>A CA351747563 NM_001354723.2:c.88G>C