{{Rsnum
|rsid=141733599
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALB
|position=73404406
|Gene_s=ALB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=4
|CLNACC=RCV000019887.1
|CLNALLE=1
|CLNDBN=ALBUMIN LARINO
|CLNHGVS=NC_000004.11:g.74270123C>T
|CLNORIGIN=1
|CLNSIG=255
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0042
|Disease=ALBUMIN LARINO
|FwdALT=T
|FwdREF=C
|GENEINFO=ALB:213
|GENE_ID=213
|GENE_NAME=ALB
|REF=C
|RSPOS=74270123
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050268000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=141733599
}}{{PMID Auto
|PMID=8022807
|Title=Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.
|OA=1
}}