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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PSPH
(R101*)
Single nucleotide variant
(nonsense)
Seizure
+1 more
GLikely pathogenic
LOC129998495, PSPH
Single nucleotide variant
(5 prime UTR variant +1 more)
Deficiency of phosphoserine phosphatase
GUncertain significance
LOC129998495, PSPH
Single nucleotide variant
(5 prime UTR variant +1 more)
Deficiency of phosphoserine phosphatase
GUncertain significance
LOC129998495, PSPH
Single nucleotide variant
(5 prime UTR variant +1 more)
Deficiency of phosphoserine phosphatase
GUncertain significance
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