Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.2583535C>ACA004880KCNQ1c.1022C>A (p.Ala341Glu)
c.641C>A (p.Ala214Glu)
ClinVar dbSNP
11g.2583535C>GCA004889KCNQ1c.1022C>G (p.Ala341Gly)
c.641C>G (p.Ala214Gly)
ClinVar dbSNP
11g.2583535C>TCA004897KCNQ1c.1022C>T (p.Ala341Val)
c.641C>T (p.Ala214Val)
ClinVar dbSNP COSMIC

Number of alleles fetched