Canonical Allele Identifier: PA2825852055
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2290132
ClinVar RCV Id: RCV002854159 RCV003991050
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Trp124Arg
CA415077941
NM_001142805.2:c.370T>A
CA415077944
NM_001142805.2:c.370T>C