Canonical Allele Identifier: PA2825852805
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1806741
ClinVar RCV Id: RCV002474170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Ser345Cys
CA415087076
NM_001142806.1:c.1034C>G