Canonical Allele Identifier: PA2827926812
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 526675
ClinVar RCV Id: RCV000631271 RCV001553666 RCV002448934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Arg82Leu
CA351750555
NM_001354723.2:c.245G>T