Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.1610901G>ACA10603005FOXC1c.456G>A (p.Trp152Ter)
ClinVar dbSNP
6g.1610901G>TCA362558863FOXC1c.456G>T (p.Trp152Cys)
ClinVar dbSNP
6g.1610901G=CA1605822558FOXC1c.456G= (p.Trp152=)
dbSNP

Number of alleles fetched