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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC105377276, MTHFD2L
(E252D +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC105377276, MTHFD2L
(K272E +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
MTHFD2L
Copy number loss
not provided
GLikely benign
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