Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_002834.4(PTPN11):c.922A>G (p.Asn308Asp) | Pathogenic | Noonan syndrome | 2018-12-10 | 1.0 | - | PTPN11 |
Showing 1 to 1 of 1 rows