Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.138946431A>GCA10654897FOXL2c.292T>C (p.Trp98Arg)
ClinVar dbSNP
3g.138946431A>TCA354706977FOXL2c.292T>A (p.Trp98Arg)
dbSNP

Number of alleles fetched