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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLCB4
(N329T)
Single nucleotide variant
(missense variant)
Auriculocondylar syndrome 1
GPathogenic
PLCB4
(R621C +1 more)
Single nucleotide variant
(missense variant)
Auriculocondylar syndrome 1
GPathogenic
PLCB4
(R621H +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GPathogenic
PLCB4
(Y623C +1 more)
Single nucleotide variant
(missense variant)
Auriculocondylar syndrome 1
GPathogenic
PLCB4
(N650H +1 more)
Single nucleotide variant
(missense variant)
Auriculocondylar syndrome 1
GPathogenic
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