Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001482.3(GATM):c.1252T>C (p.Leu418=) | Benign | AGAT deficiency | 2022-10-07 | 1.0 | - | GATM |
Showing 1 to 1 of 1 rows