Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.17387556T>GCA172332KCNJ11c.275A>C (p.Glu92Ala)
c.536A>C (p.Glu179Ala)
n.694A>C
 ClinVar dbSNP
11g.17387556T=CA1955119308KCNJ11c.275A= (p.Glu92=)
c.536A= (p.Glu179=)
n.694A=
 dbSNP

Number of alleles fetched