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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRAK1
(H71R)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GUncertain significance
TRAK1
(V190I +3 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
TRAK1
(P761L +4 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GUncertain significance
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