Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142110G>CCA020202VHLc.263G>C (p.Trp88Ser)
ClinVar dbSNP COSMIC
3g.10142110G>ACA020197VHLc.263G>A (p.Trp88Ter)
ClinVar dbSNP COSMIC

Number of alleles fetched