NM_000335.5(SCN5A):c.1308G>A (p.Glu436=) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001699792.10
Allele description [Variation Report for NM_000335.5(SCN5A):c.1308G>A (p.Glu436=)]
NM_000335.5(SCN5A):c.1308G>A (p.Glu436=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024