NM_020822.3(KCNT1):c.1704C>T (p.Asp568=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002647529.3
Allele description [Variation Report for NM_020822.3(KCNT1):c.1704C>T (p.Asp568=)]
NM_020822.3(KCNT1):c.1704C>T (p.Asp568=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024