Canonical Allele Identifier: PA2499252053
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1014141
ClinVar RCV Id: RCV001312837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Tyr165His
CA1345067433
NM_001354723.2:c.493T>C