Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150974851C>ACA005012KCNH2c.167G>T (p.Arg56Leu)
c.-11G>T (n.-11G>T)
n.390G>T
 ClinVar dbSNP gnomAD v4
7g.150974851C>TCA005006KCNH2c.167G>A (p.Arg56Gln)
c.-11G>A (n.-11G>A)
n.390G>A
 ClinVar dbSNP

Number of alleles fetched