NM_000334.4(SCN4A):c.5177A>G (p.His1726Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 1, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001552574.2
Allele description [Variation Report for NM_000334.4(SCN4A):c.5177A>G (p.His1726Arg)]
NM_000334.4(SCN4A):c.5177A>G (p.His1726Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023