| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.23424816C>A | CA389047937 | MYH7 | c.2632G>T (p.Val878Leu) n.2738G>T | ClinVar dbSNP |
| 14 | g.23424816C>G | CA012769 | MYH7 | c.2632G>C (p.Val878Leu) n.2738G>C | ClinVar dbSNP |
| 14 | g.23424816C>T | CA389047939 | MYH7 | c.2632G>A (p.Val878Met) n.2738G>A | ClinVar dbSNP |