Canonical Allele Identifier: PA353841
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 219160
ClinVar RCV Id: RCV000203508 RCV000208847 RCV001064921 RCV002433899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Tyr98Ser
CA279916
NM_000551.4:c.293A>C