Canonical Allele Identifier: PA2827926903
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1799025
ClinVar RCV Id: RCV002435996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Leu101Gln
CA351750997
NM_001354723.2:c.302T>A