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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129931979, RASAL2
(P5S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
RASAL2
(E1133* +1 more)
Single nucleotide variant
(nonsense)
Malignant tumor of prostate
GUncertain significance