Allele Registry

Canonical Allele Identifier: PA1139703191

Gene: SLC6A8 HGNC NCBI

ClinVar Variation Id: 976445

ClinVar RCV Id: RCV001253759

ClinVar Variation Id: 2049216

ClinVar RCV Id: RCV002932273

HGVS (amino-acid)	Matching Registered Transcripts
NP_005620.1:p.Ser417Arg	CA415086631 NM_005629.4:c.1249A>C CA415086636 NM_005629.4:c.1251C>A CA415086637 NM_005629.4:c.1251C>G