| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.41970533A>C | CA341236 | ATP1A3 | c.2312T>G (p.Ile771Ser) c.2273T>G (p.Ile758Ser) c.2306T>G (p.Ile769Ser) c.2183T>G (p.Ile728Ser) | ClinVar dbSNP |
| 19 | g.41970533A= | CA2336721076 | ATP1A3 | c.2312T= (p.Ile771=) c.2273T= (p.Ile758=) c.2306T= (p.Ile769=) c.2183T= (p.Ile728=) | dbSNP |