NM_172107.4(KCNQ2):c.409T>G (p.Phe137Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002282984.3
Allele description [Variation Report for NM_172107.4(KCNQ2):c.409T>G (p.Phe137Val)]
NM_172107.4(KCNQ2):c.409T>G (p.Phe137Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024