Allele Registry

Canonical Allele Identifier: PA2825852059

Gene: SLC6A8 HGNC NCBI

ClinVar RCV:

RCV000012469

ClinVar Variation:

11703

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136277.1:p.Gly132Val	CA256014 NM_001142805.2:c.395G>T