NM_001040142.2(SCN2A):c.781G>T (p.Val261Leu) AND Seizure
- Germline classification:
- Pathogenic (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001526607.2
Allele description [Variation Report for NM_001040142.2(SCN2A):c.781G>T (p.Val261Leu)]
NM_001040142.2(SCN2A):c.781G>T (p.Val261Leu)
Condition(s)
- Name:
- Seizure
- Synonyms:
- Seizures
- Identifiers:
- MedGen: C0036572; Human Phenotype Ontology: HP:0001250
Assertion and evidence details
Last Updated: Jun 23, 2024