H1850D (p.His1850Asp) variant of CR1 (Complement receptor type 1)
H1850D (p.His1850Asp) in CR1 (Complement receptor type 1) is a missense change. The record also includes published literature.
H1850D (p.His1850Asp) variant details
- p.His1850Asp
- UniProt VAR 013826
- Missense
- Cited in: Molecular identification of Knops blood group polymorphisms found in long homologous region D of complement receptor 1. (PMID 11313284)
- Cited in: Structure of the gene for the F allele of complement receptor type 1 and sequence of the coding region unique to the S… (PMID 8245463)