Allele Registry

Canonical Allele Identifier: PA2825852724

Gene: SLC6A8 HGNC NCBI

ClinVar RCV:

RCV000012463

ClinVar Variation:

11697

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136278.1:p.Gly266Arg	CA256011 NM_001142806.1:c.796G>C CA415085971 NM_001142806.1:c.796G>A