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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000314.6(PTEN):c.132C>T (p.Gly44=) | Likely Benign | PTEN hamartoma tumor syndrome | 2018-12-10 | 1.0 | - | PTEN |
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