Canonical Allele Identifier: PA2825851955
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_001136277.1:p.Gly26Arg
CA415076138
NM_001142805.2:c.76G>A
CA415076140
NM_001142805.2:c.76G>C