Canonical Allele Identifier: PA916057441
Gene: VHL HGNC NCBI

Linked Data

ClinVar Variation Id: 565557
ClinVar RCV Id: RCV000685144
ClinVar Variation Id: 2203305
ClinVar RCV Id: RCV002651638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_937799.1:p.Ser111Cys
CA351751322
NM_198156.3:c.331A>T
CA2573106137
NM_198156.3:c.330_331delinsTT