Canonical Allele Identifier: PA2825852792
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1474428
ClinVar RCV Id: RCV002005507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Arg325Cys
CA10549491
NM_001142806.1:c.973C>T