Canonical Allele Identifier: PA916057259
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 821314
ClinVar RCV Id: RCV001015609 RCV001219698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg82His
CA351750549
NM_198156.3:c.245G>A