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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_001110792.2(MECP2):c.895G>C (p.Ala299Pro) | Likely Benign | Rett syndrome | 2021-12-27 | 1.0 | - | MECP2 |
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