Canonical Allele Identifier: PA2573205662
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1392508
ClinVar RCV Id: RCV001896258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Cys174Phe
CA2529546627
NM_001354723.2:c.521G>T