Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142124G>ACA020230VHLc.277G>A (p.Gly93Ser)
ClinVar dbSNP COSMIC
3g.10142124G>TCA357106VHLc.277G>T (p.Gly93Cys)
ClinVar dbSNP gnomAD
3g.10142124G>CCA357130VHLc.277G>C (p.Gly93Arg)
ClinVar dbSNP COSMIC

Number of alleles fetched