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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNAQ
(L316V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GNAQ
(Q299H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GNAQ
(L288I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GNAQ
(Q152H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
GNAQ
(K77R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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