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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DYNLT2, ERMARD
(A23P)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
DYNLT2, ERMARD
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign