NM_000335.5(SCN5A):c.4068G>C (p.Ala1356=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003771541.2
Allele description [Variation Report for NM_000335.5(SCN5A):c.4068G>C (p.Ala1356=)]
NM_000335.5(SCN5A):c.4068G>C (p.Ala1356=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 13, 2024