Canonical Allele Identifier: PA913198345
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 624450
ClinVar RCV Id: RCV000762678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Phe406Leu
CA415086524
NM_005629.4:c.1216T>C
CA415086536
NM_005629.4:c.1218C>A
CA415086537
NM_005629.4:c.1218C>G