NM_001159699.2(FHL1):c.776A>G (p.Gln259Arg) AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 17, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002023182.6
Allele description [Variation Report for NM_001159699.2(FHL1):c.776A>G (p.Gln259Arg)]
NM_001159699.2(FHL1):c.776A>G (p.Gln259Arg)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024