Canonical Allele Identifier: PA2741924138
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2522769
ClinVar RCV Id: RCV003265460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Thr42Ala
CA415076352
NM_005629.4:c.124A>G