Showing 1 to 1 of 1 rows
See Report
Preferred Variant Title
Classification
Condition
Published Date
Version
Criteria Specification
Gene
View NM_001754.4(RUNX1):c.985G>A (p.Ala329Thr)
Likely Benign
hereditary thrombocytopenia and hematologic cancer predisposition syndrome2020-06-02
1.0
-RUNX1
Showing 1 to 1 of 1 rows