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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATL1
(F130L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ATL1
(H343D)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 3A
GUncertain significance
ATL1
(M347I)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 3A
GLikely pathogenic
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