Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.202467620T>G | CA350399729 | BMPR2 | c.349T>G (p.Cys117Gly) c.280T>G (p.Cys94Gly) n.256T>G | ClinVar dbSNP |
2 | g.202467620T>C | CA350399728 | BMPR2 | c.349T>C (p.Cys117Arg) c.280T>C (p.Cys94Arg) n.256T>C | ClinVar dbSNP |