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Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129995898, MYLIP
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
LOC129995898, MYLIP
(A19E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MYLIP
(H325fs)
Deletion
(frameshift variant)
Coronary artery atherosclerosis
GUncertain significance
LOC129995898, MYLIP
(V17A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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