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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NLRP12
(S631R)
Single nucleotide variant
(missense variant)
Familial cold autoinflammatory syndrome 2
GUncertain significance
NLRP12
(Q628H)
Single nucleotide variant
(missense variant)
Familial cold autoinflammatory syndrome 2
+1 more
GUncertain significance
NLRP12
(R370K)
Single nucleotide variant
(missense variant)
Familial cold autoinflammatory syndrome 2
GUncertain significance
NLRP12
Single nucleotide variant
(synonymous variant)
Familial cold autoinflammatory syndrome 2
+1 more
GConflicting classifications of pathogenicity
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