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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NTRK1
(L183P +1 more)
Single nucleotide variant
(missense variant)
Hereditary insensitivity to pain with anhidrosis
+1 more
GPathogenic/Likely pathogenic
NTRK1
Single nucleotide variant
(splice donor variant)
Hereditary insensitivity to pain with anhidrosis
GPathogenic
NTRK1
(S567C +2 more)
Single nucleotide variant
(missense variant)
Hereditary insensitivity to pain with anhidrosis
+3 more
GConflicting classifications of pathogenicity
NTRK1
(R725W +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
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