Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.17387226C>GCA277103KCNJ11c.605G>C (p.Gly202Ala)
c.866G>C (p.Gly289Ala)
n.1024G>C
 ClinVar dbSNP
11g.17387226C>ACA277326KCNJ11c.605G>T (p.Gly202Val)
c.866G>T (p.Gly289Val)
n.1024G>T
 ClinVar dbSNP COSMIC

Number of alleles fetched