Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.17387337A>GCA341726KCNJ11c.494T>C (p.Val165Ala)
c.755T>C (p.Val252Ala)
n.913T>C
 ClinVar dbSNP
11g.17387337A=CA1955119220KCNJ11c.494T= (p.Val165=)
c.755T= (p.Val252=)
n.913T=
 dbSNP dbSNP

Number of alleles fetched