F21V (p.Phe21Val) variant of MYL2 (P10916)
F21V (p.Phe21Val) in MYL2 (P10916) 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.
F21V (p.Phe21Val) variant details
- p.Phe21Val
- rs2499814919
- ClinGen CA386700261
- ClinVar RCV003339194
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available