P76L (p.Pro76Leu) variant of MYL2 (P10916)
P76L (p.Pro76Leu) in MYL2 (P10916) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
P76L (p.Pro76Leu) variant details
- p.Pro76Leu
- Ensembl rs868354141
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available