NM_172201.2(KCNE2):c.193G>A (p.Val65Met) AND Congenital long QT syndrome
- Germline classification:
- not provided (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000058364.5
Allele description [Variation Report for NM_172201.2(KCNE2):c.193G>A (p.Val65Met)]
NM_172201.2(KCNE2):c.193G>A (p.Val65Met)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024