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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FLCN
(R350Q +1 more)
Single nucleotide variant
(missense variant)
not specified
+7 more
GConflicting classifications of pathogenicity
FLCN
(Q324R +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
FLCN
(Y95C)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome 1
+3 more
GUncertain significance
FLCN
(A64T)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome 1
+3 more
GConflicting classifications of pathogenicity
FLCN
(R57Q)
Single nucleotide variant
(missense variant)
Birt-Hogg-Dube syndrome 1
+3 more
GConflicting classifications of pathogenicity
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