Canonical Allele Identifier: PA2825852271
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_001136277.1:p.Pro380Leu
CA415086230
NM_001142805.2:c.1139C>T