P26L (p.Pro26Leu) variant of ALPL (P05186)
P26L (p.Pro26Leu) in ALPL (P05186) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hypophosphatasia. The record also includes structural context.
P26L (p.Pro26Leu) variant details
- p.Pro26Leu
- NCI-TCGA Cosmic COSV6637
- NCI-TCGA Cosmic COSV6638
- cosmic curated COSV66380
- Uncertain significance
- Hypophosphatasia
- Missense
- ClinVar: Uncertain significance (Hypophosphatasia)
- UniProt: Uncertain significance
- Structural context available