NM_001165963.4(SCN1A):c.5404G>A (p.Glu1802Lys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002552875.5
Allele description [Variation Report for NM_001165963.4(SCN1A):c.5404G>A (p.Glu1802Lys)]
NM_001165963.4(SCN1A):c.5404G>A (p.Glu1802Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 12, 2024