| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.63957443C>T | CA16043536 | SCN4A | c.2095G>A (p.Ala699Thr) | ClinVar dbSNP gnomAD v4 |
| 17 | g.63957443C= | CA2270168670 | SCN4A | c.2095G= (p.Ala699=) | dbSNP |
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.63957443C>T | CA16043536 | SCN4A | c.2095G>A (p.Ala699Thr) | ClinVar dbSNP gnomAD v4 |
| 17 | g.63957443C= | CA2270168670 | SCN4A | c.2095G= (p.Ala699=) | dbSNP |