Canonical Allele Identifier: PA2741867955
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 2934106
ClinVar RCV Id: RCV003795856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Val119Glu
CA2740090912
NM_001354723.2:c.356T>A