{{Rsnum
|rsid=387906525
|Chromosome=1
|position=21577632
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=ALPL
|Gene_s=ALPL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000014665.23
|CLNALLE=1
|CLNDBN=Infantile hypophosphatasia
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1150:C0268412:241500:55236002
|CLNHGVS=NC_000001.11:g.21577632delT
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_000478.4:c.1559delT; 171760.0012
|Disease=Infantile hypophosphatasia
|FwdREF=T
|REF=CT
|RSPOS=21577631
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSF;REF;ASP;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060001205000002110200
|WGT=1
|dbSNPBuildID=137
|rsid=387906525
|GENEINFO=ALPL:249
|GENE_ID=249
|GENE_NAME=ALPL
|CLNORIGIN=1
}}