| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CYP26C1, LOC130004371 (G177R) | Single nucleotide variant (missense variant) | not specified | |
| | CYP26C1, LOC130004371 (D183H) | Single nucleotide variant (missense variant) | not specified | |
| | CYP26C1, LOC130004371 (A184T) | Single nucleotide variant (missense variant) | not specified | |
| | CYP26C1, LOC130004371 (R191L) | Single nucleotide variant (missense variant) | not specified | |
| | CYP26C1, LOC130004371 (A211G) | Single nucleotide variant (missense variant) | not specified | |
| | CYP26C1, LOC130004371 (P229A) | Single nucleotide variant (missense variant) | not specified | |
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