Canonical Allele Identifier: PA2825852201
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 420991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Gln304His
CA16621223
NM_001142805.2:c.912G>C
CA415084328
NM_001142805.2:c.912G>T