Canonical Allele Identifier: PA916056975
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_937799.1:p.Gly30Arg
CA70042258
NM_198156.3:c.88G>A
CA351747563
NM_198156.3:c.88G>C