NM_015443.4(KANSL1):c.1921A>G (p.Ile641Val) AND Koolen-de Vries syndrome
Clinical significance:Benign (Last evaluated: Oct 1, 2020)
Review status:
- Based on:
- 1 submission [Details]
- Record status:
- current
- Accession:
- RCV001522679.2
Allele description [Variation Report for NM_015443.4(KANSL1):c.1921A>G (p.Ile641Val)]
NM_015443.4(KANSL1):c.1921A>G (p.Ile641Val)
Condition(s)
Assertion and evidence details
Last Updated: Jun 3, 2022