Canonical Allele Identifier: PA2825851993
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1385998
ClinVar RCV Id: RCV001889111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Pro50Ser
CA415076512
NM_001142805.2:c.148C>T