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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000257.4(MYH7):c.2080C>T (p.Arg694Cys) | Likely Pathogenic | hypertrophic cardiomyopathy | 2022-07-30 | 1.0 | - | MYH7 |
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