Canonical Allele Identifier: PA2829609566
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066434
ClinVar RCV Id: RCV003991438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Pro397Leu
CA415086358
NM_005629.4:c.1190C>T