NM_001349253.2(SCN11A):c.2478G>A (p.Glu826=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002542164.10
Allele description [Variation Report for NM_001349253.2(SCN11A):c.2478G>A (p.Glu826=)]
NM_001349253.2(SCN11A):c.2478G>A (p.Glu826=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024