Canonical Allele Identifier: PA2825851976
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2749829
ClinVar RCV Id: RCV003511689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Leu40Met
CA415076320
NM_001142805.2:c.118C>A