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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126807212, TLL1
(R467C)
Single nucleotide variant
(missense variant)
Atrial septal defect 6
GUncertain significance
TLL1
(V557L)
Single nucleotide variant
(missense variant)
Atrial septal defect 6
GUncertain significance
TLL1
(L682I)
Single nucleotide variant
(missense variant)
Atrial septal defect 6
GUncertain significance
TLL1
(R847Q)
Single nucleotide variant
(missense variant)
Atrial septal defect 6
GUncertain significance
TLL1
(R928Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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