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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PPP1CA
(P71R +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PPP1CA
(E56G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
PPP1CA
(S20P)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
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