ClinVar Miner

Submissions for variant NM_004304.5(ALK):c.1201_1218dup (p.Tyr406_Ile407insArgValAlaLeuGluTyr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005024470 SCV005649276 uncertain significance Neuroblastoma, susceptibility to, 3 2024-02-17 criteria provided, single submitter clinical testing

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