Canonical Allele Identifier: PA2825852023
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 11700
ClinVar RCV Id: RCV001508970 RCV000012466
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Gly87Arg
CA256012
NM_001142805.2:c.259G>A
CA415077143
NM_001142805.2:c.259G>C