Allele Registry

Canonical Allele Identifier: PA2825852763

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_001136278.1:p.Ser302Arg	CA415086631 NM_001142806.1:c.904A>C CA415086636 NM_001142806.1:c.906C>A CA415086637 NM_001142806.1:c.906C>G