APOA5 Gene Details
Disease Name: Familial chylomicronemia syndrome
Chromosomal Location: Chromosome 11, NC_000011.10
Nucleotide Accession: AF202889.1 AF202890.1 AK292739.1 AK315229.1 AY358749.1 AY422949.1 AY555191.1 BC101787.1 BC101789.1 CH471065.1 CM000262.1 DQ030388.1 DR004147.1 EF444949.1 KJ401315.1 NC_000011.10 NC_060935.1 NG_015894.2 NG_051344.1 NM_001145311.2 NM_001159736.2
Mode of Inheritence: Autosomal recessive
