Canonical Allele Identifier: PA645463520
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 410221
ClinVar RCV Id: RCV000477133

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Gly39Asp
CA16616458
NM_005629.4:c.116G>A