NM_001159699.2(FHL1):c.816C>A (p.Ser272=) AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 23, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001472604.7
Allele description [Variation Report for NM_001159699.2(FHL1):c.816C>A (p.Ser272=)]
NM_001159699.2(FHL1):c.816C>A (p.Ser272=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024