Allele Registry

Canonical Allele Identifier: PA2825852789

Gene: SLC6A8 HGNC NCBI

ClinVar Allele:

929599

ClinVar RCV:

RCV001217348

RCV001551569

ClinVar Variation:

946475

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136278.1:p.Tyr323Phe	CA415086789 NM_001142806.1:c.968A>T