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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130008965, P2RX4
(V43L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130008965, P2RX4
(I44T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130008965, P2RX4
(L38F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130008965, P2RX4
(G3C)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
LOC130008965, P2RX4
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
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