Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.70175935A>G | CA400862582 | KCNJ2 | c.896A>G (p.Glu299Gly) | ClinVar dbSNP |
17 | g.70175935A>T | CA302052 | KCNJ2 | c.896A>T (p.Glu299Val) | ClinVar dbSNP |
17 | g.70175935A= | CA2272996730 | KCNJ2 | c.896A= (p.Glu299=) | dbSNP |