NM_000335.5(SCN5A):c.5779T>G (p.Phe1927Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 19, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003656785.1
Allele description
NM_000335.5(SCN5A):c.5779T>G (p.Phe1927Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 16, 2024