Canonical Allele Identifier: PA2573205629
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1482705
ClinVar RCV Id: RCV001995759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Thr132Ile
CA2573136101
NM_001354723.2:c.395C>T