Canonical Allele Identifier: PA108421
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223225
ClinVar RCV Id: RCV000208789 RCV003278699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000542.1:p.Cys162Tyr
CA357010
NM_000551.4:c.485G>A