Canonical Allele Identifier: PA916003183
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 643295
ClinVar Variation Id: 2166077
ClinVar RCV Id: RCV003090308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Gly26Arg
CA415076138
NM_005629.4:c.76G>A
CA415076140
NM_005629.4:c.76G>C