Canonical Allele Identifier: PA2825852760
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503222
ClinVar RCV Id: RCV002022714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Asp301Gly
CA415086626
NM_001142806.1:c.902A>G