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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTC21A
Single nucleotide variant
(intron variant)
Spermatogenic failure 37
GPathogenic
TTC21A
Deletion
(nonsense +1 more)
Spermatogenic failure 37
GPathogenic
TTC21A
(Y114C)
Single nucleotide variant
(missense variant +1 more)
Spermatogenic failure 37
GPathogenic
TTC21A
(Q777* +3 more)
Single nucleotide variant
(nonsense +1 more)
Spermatogenic failure 37
GPathogenic
TTC21A
Single nucleotide variant
(splice donor variant)
Spermatogenic failure 37
GPathogenic
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