Allele Registry

Canonical Allele Identifier: PA2825852300

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_001136277.1:p.Ser407Arg	CA415086631 NM_001142805.2:c.1219A>C CA415086636 NM_001142805.2:c.1221C>A CA415086637 NM_001142805.2:c.1221C>G