Canonical Allele Identifier: PA2825852278
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066434
ClinVar RCV Id: RCV003991438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Pro387Leu
CA415086358
NM_001142805.2:c.1160C>T