Canonical Allele Identifier: PA2825851981
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Pro43Ser
CA415076372
NM_001142805.2:c.127C>T