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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SZT2
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
SZT2
(F1343L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SZT2
(R1965C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SZT2
(C2396Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SZT2
(H3030R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
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