NM_001040142.2(SCN2A):c.5752C>T (p.Arg1918Cys) AND History of neurodevelopmental disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 6, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000718780.1
Allele description
NM_001040142.2(SCN2A):c.5752C>T (p.Arg1918Cys)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
Assertion and evidence details
Last Updated: Oct 22, 2022