Canonical Allele Identifier: PA2499252043
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1042971
ClinVar RCV Id: RCV001347010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Asp156Tyr
CA1345067355
NM_001354723.2:c.466G>T