Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.37739473A>GCA214361HNF1Bc.511T>C (p.Trp171Arg)
ClinVar dbSNP
17g.37739473A>TCA398751173HNF1Bc.511T>A (p.Trp171Arg)
dbSNP
17g.37739473A=CA3223295346HNF1Bc.511T= (p.Trp171=)
dbSNP

Number of alleles fetched