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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARPC1B
(R103H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ARPC1B
(C162G)
Single nucleotide variant
(missense variant)
Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
+1 more
GUncertain significance
ARPC1B
Single nucleotide variant
(synonymous variant)
Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
+1 more
GPathogenic
ARPC1B
(V329I)
Single nucleotide variant
(missense variant)
Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
GUncertain significance
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