NM_001040142.2(SCN2A):c.713T>C (p.Val238Ala) AND Developmental and epileptic encephalopathy, 11
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002283640.1
Allele description [Variation Report for NM_001040142.2(SCN2A):c.713T>C (p.Val238Ala)]
NM_001040142.2(SCN2A):c.713T>C (p.Val238Ala)
Condition(s)
Assertion and evidence details
Last Updated: Aug 5, 2023