Canonical Allele Identifier: PA2499252050
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 1034798
ClinVar RCV Id: RCV001337572
ClinVar Variation Id: 1550054
ClinVar RCV Id: RCV002189562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341652.1:p.Gly161Arg
CA1345067404
NM_001354723.2:c.481G>A
CA2573136122
NM_001354723.2:c.481G>C