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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CFP
(D299N)
Single nucleotide variant
(missense variant)
CFP-related condition
+1 more
GBenign/Likely benign
CFP
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CFP
(G194R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CFP
(V53M)
Single nucleotide variant
(missense variant)
not provided
GBenign
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