Links from Orgtrack
Items: 2
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Microcephaly 27, primary, autosomal dominant | |
| | | Single nucleotide variant (missense variant) | Congenital secretory sodium diarrhea 8 | |
Click to view in NCBI Gene