Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.126693273C>TCA254055LMX1Bc.691C>T (p.Arg231Ter)
c.622C>T (p.Arg208Ter)
 ClinVar dbSNP gnomAD v2
9g.126693273C=CA1879478563LMX1Bc.691C= (p.Arg231=)
c.622C= (p.Arg208=)
 dbSNP

Number of alleles fetched