Canonical Allele Identifier: PA2825852293
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 976446
ClinVar RCV Id: RCV001253760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Leu401Ser
CA415086584
NM_001142805.2:c.1202T>C