Canonical Allele Identifier: PA2573205666
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1469973
ClinVar RCV Id: RCV001963962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Glu182Lys
CA2573136137
NM_001354723.2:c.544G>A