Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.209801409G>ACA252758IRF6c.5C>T (p.Ala2Val)
c.-112+4538C>T (n.-112+4538C>T)
ClinVar dbSNP COSMIC
1g.209801409G=CA1140496146IRF6c.5C= (p.Ala2=)
c.-112+4538C= (n.-112+4538C=)
dbSNP

Number of alleles fetched