NM_001159699.2(FHL1):c.767A>C (p.Tyr256Ser) AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001896871.2
Allele description [Variation Report for NM_001159699.2(FHL1):c.767A>C (p.Tyr256Ser)]
NM_001159699.2(FHL1):c.767A>C (p.Tyr256Ser)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023