Canonical Allele Identifier: PA280298
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 36905
ClinVar RCV Id: RCV000030589 RCV000492408 RCV000533687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Tyr175Cys
CA020462
NM_000551.4:c.524A>G