Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001083962.2(TCF4):c.504A>G (p.Val168=) | Benign | Pitt-Hopkins syndrome | 2022-06-30 | 1.0 | - | TCF4 |
Showing 1 to 1 of 1 rows