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 170932516 NP_002850 rs4767884页。HIS73ASP多态性dbSNP NULL NULL rs4767884