Canonical Allele Identifier: PA2825851988
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436501
ClinVar RCV Id: RCV002002122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Val49Ala
CA415076503
NM_001142805.2:c.146T>C