Canonical Allele Identifier: PA108439
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2238
ClinVar RCV Id: RCV000002326 RCV001052383 RCV001023261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Gln164Arg
CA020429
NM_000551.4:c.491A>G