Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.126693243C>TCA254044LMX1Bc.661C>T (p.Arg221Ter)
c.592C>T (p.Arg198Ter)
 ClinVar dbSNP gnomAD v4
9g.126693243C=CA1879478518LMX1Bc.661C= (p.Arg221=)
c.592C= (p.Arg198=)
 dbSNP

Number of alleles fetched