Canonical Allele Identifier: PA2827926811
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 193118
ClinVar RCV Id: RCV000173161 RCV000724457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg82Pro
CA020159
NM_001354723.2:c.245G>C