NM_000747.3(CHRNB1):c.909A>G (p.Leu303=) AND Congenital myasthenic syndrome 2A
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000794394.6
Allele description [Variation Report for NM_000747.3(CHRNB1):c.909A>G (p.Leu303=)]
NM_000747.3(CHRNB1):c.909A>G (p.Leu303=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024