The Novel Allele, HLA‐DPA1*01:213 , With a Non‐Synonymous Mutation in Exon 3

Key Points

• The research aims to characterize the novel HLA-DPA1*01:213 allele and its mutation.
• Identified HLA-DPA1*01:213 allele
• Analyzed the specific nucleotide substitution
• Examined the impact of the mutation in exon 3
• HLA-DPA1*01:213 allele contains a unique nucleotide substitution
• The mutation occurs at codon 163
• Substitution changes threonine to arginine (TGC to CGC)