| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | AFP, LOC126807077 (S445L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | AFP, LOC126807077 (A318V +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene