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Items: 5

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