Allele Registry

Canonical Allele Identifier: PA891852059

Gene: SLC6A8 HGNC NCBI

ClinVar RCV:

RCV000692670

RCV001830511

ClinVar Variation:

571505

HGVS (amino-acid)	Matching Registered Transcripts
NP_005620.1:p.Gly9Val	CA415075922 NM_005629.4:c.26G>T