NM_001267550.2(TTN):c.61696G>A (p.Val20566Ile) AND Autosomal recessive limb-girdle muscular dystrophy type 2J
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000307537.5
Allele description [Variation Report for NM_001267550.2(TTN):c.61696G>A (p.Val20566Ile)]
NM_001267550.2(TTN):c.61696G>A (p.Val20566Ile)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024