| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130062850, R3HDM4 (P18L) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130062850, R3HDM4 (G20W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130062850, R3HDM4 (E15D) | Single nucleotide variant (missense variant) | not specified | |
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