A69G (p.Ala69Gly) variant of FHL1 (Q13642)
A69G (p.Ala69Gly) in FHL1 (Q13642) 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.
A69G (p.Ala69Gly) variant details
- p.Ala69Gly
- rs2521263387
- ClinGen CA414607993
- ClinVar RCV003147265
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available