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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERLIN1
(V180I +2 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary spastic paraplegia 62
GUncertain significance
ERLIN1, LOC130004521
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
ERLIN1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
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