Canonical Allele Identifier: PA645463646
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 436771

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Ala388Thr
CA10549443
NM_005629.4:c.1162G>A