Allele Registry

Canonical Allele Identifier: PA2825852839

Gene: SLC6A8 HGNC NCBI

ClinVar RCV:

RCV000012470

ClinVar Variation:

11704

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136278.1:p.Cys376Trp	CA256015 NM_001142806.1:c.1128C>G