Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150951511C>TCA005807KCNH2c.1882G>A (p.Gly628Ser)
c.862G>A (p.Gly288Ser)
c.1534G>A (p.Gly512Ser)
c.1582G>A (p.Gly528Ser)
c.1732G>A (p.Gly578Ser)
c.1705G>A (p.Gly569Ser)
ClinVar dbSNP
7g.150951511C>GCA005813KCNH2c.1882G>C (p.Gly628Arg)
c.862G>C (p.Gly288Arg)
c.1534G>C (p.Gly512Arg)
c.1582G>C (p.Gly528Arg)
c.1732G>C (p.Gly578Arg)
c.1705G>C (p.Gly569Arg)
ClinVar dbSNP

Number of alleles fetched