Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150974797G>CCA006358KCNH2c.221C>G (p.Thr74Arg)
c.44C>G (p.Thr15Arg)
n.444C>G
ClinVar dbSNP
7g.150974797G>ACA006365KCNH2c.221C>T (p.Thr74Met)
c.44C>T (p.Thr15Met)
n.444C>T
ClinVar dbSNP

Number of alleles fetched