{{Rsnum
|rsid=121908556
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SCN4A
|position=63957515
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCN4A
}}{{omim
|id=603967
|rsnum=121908556
|variant=0022
}}
{{omim
|id=603967
|rsnum=121908556
|variant=0024
}}{{ClinVar
|rsid=121908556
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=62034875
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCN4A:6329
|GENE_NAME=SCN4A
|GENE_ID=6329
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000017.10:g.62034875G>A; NC_000017.10:g.62034875G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603967.0024; 603967.0022
|CLNSIG=5
|CLNCUI=C1868433
|CLNDBN=Normokalemic periodic paralysis, potassium-sensitive
|Disease=Normokalemic periodic paralysis
|CLNACC=RCV000006263.2; RCV000006281.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1868433
}}