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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTRC
(W55*)
Single nucleotide variant
(nonsense)
Hereditary pancreatitis
GPathogenic
CTRC
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
CTRC
(A73T)
Single nucleotide variant
(missense variant)
Hereditary pancreatitis
GConflicting classifications of pathogenicity
CTRC
Deletion
(inframe_deletion)
not specified
+2 more
GPathogenic
CTRC
(R254W)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity; association
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