[MIM*103600] The autosomal dominant condition of having serum albumin of a variant type that differs in mobility on electrophoresis from the usual type A; affects people who are heterozygous or homozygous for one of the alleles for variant albumin types, a genetic polymorphism without known clinical significance.inherited albumin variants, under variant. [allo- + albumin + G. haima, blood, + -ia]
