Allele Registry

Canonical Allele Identifier: PA104632

Gene: SLC6A8 HGNC NCBI

ClinVar RCV:

RCV000055919

ClinVar Variation:

65693

HGVS (amino-acid)	Matching Registered Transcripts
NP_005620.1:p.Pro554Leu	CA345036 NM_005629.4:c.1661C>T