NM_001164508.2(NEB):c.426T>C (p.Asp142=) AND Nemaline myopathy 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000920371.16
Allele description [Variation Report for NM_001164508.2(NEB):c.426T>C (p.Asp142=)]
NM_001164508.2(NEB):c.426T>C (p.Asp142=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024