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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPD1
(K418T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
HSPD1
(N208T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
HSPD1
(F32C)
Single nucleotide variant
(missense variant)
Spastic paraplegia
+1 more
GUncertain significance
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