Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150974897C>ACA004285KCNH2c.121G>T (p.Val41Phe)
c.-57G>T (n.-57G>T)
n.344G>T
 ClinVar dbSNP
7g.150974897C>GCA16042697KCNH2c.121G>C (p.Val41Leu)
c.-57G>C (n.-57G>C)
n.344G>C
 ClinVar dbSNP

Number of alleles fetched