NM_001164508.2(NEB):c.1187C>T (p.Ala396Val) AND Nemaline myopathy 2
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 18, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000695689.5
Allele description [Variation Report for NM_001164508.2(NEB):c.1187C>T (p.Ala396Val)]
NM_001164508.2(NEB):c.1187C>T (p.Ala396Val)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024