Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.17387595C>ACA119833KCNJ11c.236G>T (p.Cys79Phe)
c.497G>T (p.Cys166Phe)
n.655G>T
 ClinVar dbSNP
11g.17387595C>TCA341720KCNJ11c.236G>A (p.Cys79Tyr)
c.497G>A (p.Cys166Tyr)
n.655G>A
 ClinVar dbSNP

Number of alleles fetched