Canonical Allele Identifier: PA2825851936
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 934136
ClinVar RCV Id: RCV001202474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Gly9Cys
CA415075918
NM_001142805.2:c.25G>T