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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCYT1B
(M310L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PCYT1B
(K144R +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PCYT1B
(P40T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PCYT1B
(E21K)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
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