Entrez_Gene_（基因ID）HUGO_Symbol Entrez_Protein_（GI）Protein_Accession Chosen_Mutation_ID HGVS突变_Class突变_Source Disease OMIM_Link Swiss-Prot_Link dbSNP_Link5829 PXN 317373486 P49023 VAR_065099 p.多态Swiss-Prot NULL VAR_065099 rs47678845829 PXN 317373486 P49023 rs4767884页。HIS73ASP多态性dbSNP NULL NULL rs4767884