NM_020822.3(KCNT1):c.2892C>T (p.Phe964=) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000548689.18
Allele description [Variation Report for NM_020822.3(KCNT1):c.2892C>T (p.Phe964=)]
NM_020822.3(KCNT1):c.2892C>T (p.Phe964=)
Condition(s)
Assertion and evidence details
Last Updated: Dec 22, 2024