Canonical Allele Identifier: PA2499252045
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1024028
ClinVar RCV Id: RCV001324160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Trp159Cys
CA1345067387
NM_001354723.2:c.477G>T