NM_001040142.2(SCN2A):c.2661A>G (p.Val887=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000555957.9
Allele description [Variation Report for NM_001040142.2(SCN2A):c.2661A>G (p.Val887=)]
NM_001040142.2(SCN2A):c.2661A>G (p.Val887=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 16, 2024