Canonical Allele Identifier: PA2827926891
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 223176
ClinVar RCV Id: RCV000208825 RCV001218807 RCV001357107
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Tyr98Cys
CA357072
NM_001354723.2:c.293A>G