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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126861127, PPFIBP2
(S324L +5 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126861127, PPFIBP2
(P266L +5 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
LOC126861127, PPFIBP2
(K204N +5 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC126861127, PPFIBP2
(E281K +5 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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