Canonical Allele Identifier: PA1139703008
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 940774
ClinVar RCV Id: RCV001210427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Gln114His
CA415077745
NM_005629.4:c.342G>C
CA415077746
NM_005629.4:c.342G>T