Canonical Allele Identifier: PA2825852037
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066438
ClinVar RCV Id: RCV003991442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Gly101Arg
CA415077486
NM_001142805.2:c.301G>A
CA415077489
NM_001142805.2:c.301G>C