Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001110792.2(MECP2):c.877G>A (p.Ala293Thr) | Benign | Rett syndrome | 2023-12-08 | 1.0 | - | MECP2 |
Showing 1 to 1 of 1 rows