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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001323289.2(CDKL5):c.1002T>C (p.Ala334=) | Benign | CDKL5 disorder | 2023-03-31 | 1.0 | - | CDKL5 |
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