Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.209795344G>ACA16603558IRF6c.454C>T (p.Gln152Ter)
c.169C>T (p.Gln57Ter)
ClinVar dbSNP
1g.209795344G=CA2484367235IRF6c.454C= (p.Gln152=)
c.169C= (p.Gln57=)
dbSNP

Number of alleles fetched