Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.37739455G>ACA122597HNF1Bc.529C>T (p.Arg177Ter)
 ClinVar dbSNP
17g.37739455G>TCA499603852HNF1Bc.529C>A (p.Arg177=)
 dbSNP

Number of alleles fetched