Canonical Allele Identifier: PA2825852294
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1285397
ClinVar RCV Id: RCV001706753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Leu402Pro
CA415086592
NM_001142805.2:c.1205T>C