G53V (p.Gly53Val) variant of MYPN (Myopalladin)
G53V (p.Gly53Val) in MYPN (Myopalladin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
G53V (p.Gly53Val) variant details
- p.Gly53Val
- rs2042243303
- ClinGen CA377103724
- ClinVar RCV002398407
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available