A13T (p.Ala13Thr) variant of MYL3 (Myosin light chain 3)
A13T (p.Ala13Thr) in MYL3 (Myosin light chain 3) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hypertrophic cardiomyopathy. The record also includes structural context.
A13T (p.Ala13Thr) variant details
- p.Ala13Thr
- cosmic curated COSV52768
- Uncertain significance
- Hypertrophic cardiomyopathy
- Missense
- ClinVar: Uncertain significance (Hypertrophic cardiomyopathy)
- UniProt: Uncertain significance
- Structural context available