Canonical Allele Identifier: PA2580228823
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2013873
ClinVar RCV Id: RCV002829732
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Ser179Leu
CA2580068447
NM_001354723.2:c.536C>T