Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28768034G>ACA389475799FOXG1c.755G>A (p.Gly252Asp)
ClinVar dbSNP
14g.28768034G>TCA172191FOXG1c.755G>T (p.Gly252Val)
ClinVar dbSNP

Number of alleles fetched