ClinVar Miner

Submissions for variant NM_003977.4(AIP):c.987C>T (p.Ser329=)

dbSNP: rs267606587
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000034116 SCV000058046 not provided Somatotroph adenoma no assertion provided literature only

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