Canonical Allele Identifier: PA2825852046
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2745591
ClinVar RCV Id: RCV003511584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Glu109Asp
CA415077647
NM_001142805.2:c.327G>C
CA415077650
NM_001142805.2:c.327G>T