Allele Registry

Canonical Allele Identifier: PA2825852685

Gene: SLC6A8 HGNC NCBI

ClinVar RCV:

RCV000012468

ClinVar Variation:

11702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136278.1:p.Cys222Trp	CA256013 NM_001142806.1:c.666C>G