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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130065540, NAPB
(M1R)
Single nucleotide variant
(missense variant +3 more)
Developmental and epileptic encephalopathy-107
GUncertain significance
LOC130065540, NAPB
(E18K)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
LOC130065540, NAPB
(A4G)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
NAPB, LOC130065540
(K22R)
Single nucleotide variant
(missense variant +2 more)
NAPB-related condition
+1 more
GBenign
NAPB
Single nucleotide variant
(splice donor variant)
Malignant tumor of prostate
GUncertain significance
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