NM_014874.4(MFN2):c.299C>G (p.Ala100Gly) AND Charcot-Marie-Tooth disease
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000790051.2
Allele description [Variation Report for NM_014874.4(MFN2):c.299C>G (p.Ala100Gly)]
NM_014874.4(MFN2):c.299C>G (p.Ala100Gly)
Condition(s)
Assertion and evidence details
Last Updated: Aug 4, 2024