Canonical Allele Identifier: PA104621
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361089
ClinVar RCV Id: RCV001874229 RCV003128822
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Pro390Leu
CA415086230
NM_005629.4:c.1169C>T