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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130066790, RRP1
(N20S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
LOC130066790, RRP1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign