Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150950216G>CCA16616753KCNH2c.2350C>G (p.Arg784Gly)
c.1330C>G (p.Arg444Gly)
c.2002C>G (p.Arg668Gly)
c.2050C>G (p.Arg684Gly)
c.2200C>G (p.Arg734Gly)
c.2173C>G (p.Arg725Gly)
dbSNP
7g.150950216G>ACA006462KCNH2c.2350C>T (p.Arg784Trp)
c.1330C>T (p.Arg444Trp)
c.2002C>T (p.Arg668Trp)
c.2050C>T (p.Arg684Trp)
c.2200C>T (p.Arg734Trp)
c.2173C>T (p.Arg725Trp)
ClinVar dbSNP gnomAD

Number of alleles fetched