NM_000335.5(SCN5A):c.1743G>A (p.Ser581=) AND SCN5A-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- May 3, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004544290.1
Allele description [Variation Report for NM_000335.5(SCN5A):c.1743G>A (p.Ser581=)]
NM_000335.5(SCN5A):c.1743G>A (p.Ser581=)
Condition(s)
- Name:
- SCN5A-related disorder
- Identifiers:
Assertion and evidence details
Last Updated: Sep 29, 2024