Canonical Allele Identifier: PA2829609393
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066438
ClinVar RCV Id: RCV003991442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Gly101Arg
CA415077486
NM_005629.4:c.301G>A
CA415077489
NM_005629.4:c.301G>C