NM_001159699.2(FHL1):c.427T>C (p.Phe143Leu) AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000800282.7
Allele description [Variation Report for NM_001159699.2(FHL1):c.427T>C (p.Phe143Leu)]
NM_001159699.2(FHL1):c.427T>C (p.Phe143Leu)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024