Allele Registry

Canonical Allele Identifier: PA104590

Gene: SLC6A8 HGNC NCBI

ClinVar RCV:

RCV000012463

ClinVar Variation:

11697

HGVS (amino-acid)	Matching Registered Transcripts
NP_005620.1:p.Gly381Arg	CA256011 NM_005629.4:c.1141G>C CA415085971 NM_005629.4:c.1141G>A