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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLAT
(E129K +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC130000296, PLAT
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC130000295, PLAT
(R221C +2 more)
Single nucleotide variant
(missense variant)
Abnormal bleeding
+1 more
GUncertain significance
PLAT
(G494A +2 more)
Single nucleotide variant
(missense variant)
Thrombocytopenia
+1 more
GUncertain significance
LOC130000296, PLAT
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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