NM_001040142.2(SCN2A):c.2273A>G (p.Asp758Gly) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 5, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001228874.7
Allele description [Variation Report for NM_001040142.2(SCN2A):c.2273A>G (p.Asp758Gly)]
NM_001040142.2(SCN2A):c.2273A>G (p.Asp758Gly)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024