Canonical Allele Identifier: PA2499252024
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1002607
ClinVar RCV Id: RCV001299056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Pro118Gln
CA1345067140
NM_001354723.2:c.353C>A