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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRYM
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
CRYM
(A194T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CRYM
(E175L)
Indel
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
CRYM
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CRYM, LOC130058620
(R3L)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
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