Showing 1 to 1 of 1 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000419.4(ITGA2B):c.2965G>A (p.Ala989Thr) | Likely Benign | Glanzmann's thrombasthenia | 2021-01-28 | 1.0 | - | ITGA2B |
Showing 1 to 1 of 1 rows