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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_001042537.1(SLC9A6):c.25G>T (p.Ala9Ser) | Benign | Christianson syndrome | 2021-05-17 | 1.0 | - | SLC9A6 |
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