Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.10142038G>ACA020083VHLc.191G>A (p.Arg64His)
 ClinVar dbSNP gnomAD v4
3g.10142038G>CCA020089VHLc.191G>C (p.Arg64Pro)
 ClinVar dbSNP COSMIC
3g.10142038G=CA1345065602VHLc.191G= (p.Arg64=)
 dbSNP dbSNP

Number of alleles fetched