Canonical Allele Identifier: PA916057433
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 411972
ClinVar RCV Id: RCV000458083 RCV002269278 RCV001019385 RCV002489087 RCV004001987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Arg108His
CA040275
NM_198156.3:c.323G>A