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See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
---|---|---|---|---|---|---|---|
View | NM_000441.2(SLC26A4):c.147C>G (p.Ser49Arg) | Likely Benign | Pendred syndrome | 2019-10-31 | 1.0 | - | SLC26A4 |
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