NM_001040142.2(SCN2A):c.1901T>C (p.Val634Ala) AND multiple conditions
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jul 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000764279.4
Allele description [Variation Report for NM_001040142.2(SCN2A):c.1901T>C (p.Val634Ala)]
NM_001040142.2(SCN2A):c.1901T>C (p.Val634Ala)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024