G42A (p.Gly42Ala) variant of MYL2 (P10916)
G42A (p.Gly42Ala) in MYL2 (P10916) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G42A (p.Gly42Ala) variant details
- p.Gly42Ala
- TOPMed rs863225117
- gnomAD rs863225117
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available