NM_001159699.2(FHL1):c.597C>G (p.Ala199=) AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003832365.2
Allele description [Variation Report for NM_001159699.2(FHL1):c.597C>G (p.Ala199=)]
NM_001159699.2(FHL1):c.597C>G (p.Ala199=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024