Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150974812A>GCA006187KCNH2c.206T>C (p.Leu69Pro)
c.29T>C (p.Leu10Pro)
n.429T>C
 ClinVar dbSNP
7g.150974812A>TCA369865614KCNH2c.206T>A (p.Leu69Gln)
c.29T>A (p.Leu10Gln)
n.429T>A
 ClinVar dbSNP

Number of alleles fetched