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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
STIM1
(A163D +2 more)
Single nucleotide variant
(missense variant +3 more)
not provided
+3 more
GUncertain significance
STIM1
(G149C +5 more)
Single nucleotide variant
(missense variant +1 more)
Stormorken syndrome
+3 more
GUncertain significance
STIM1
(R530C +9 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+3 more
GConflicting classifications of pathogenicity
STIM1
(N394S +9 more)
Single nucleotide variant
(missense variant +2 more)
Myopathy with tubular aggregates
+3 more
GUncertain significance
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