Canonical Allele Identifier: PA2580334359
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1806741
ClinVar RCV Id: RCV002474170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Ser460Cys
CA415087076
NM_005629.4:c.1379C>G