NM_000335.5(SCN5A):c.4892G>A (p.Arg1631His) AND Conduction system disorder
- Germline classification:
- not provided (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000058723.3
Allele description [Variation Report for NM_000335.5(SCN5A):c.4892G>A (p.Arg1631His)]
NM_000335.5(SCN5A):c.4892G>A (p.Arg1631His)
Condition(s)
- Name:
- Conduction system disorder
- Synonyms:
- Cardiac conduction disease; Cardiac conduction defect, nonspecific
- Identifiers:
- EFO: EFO_0005137; MONDO: MONDO:0005449; MedGen: C2748542
Assertion and evidence details
Last Updated: Oct 8, 2024