Canonical Allele Identifier: PA1139703183
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 976446
ClinVar RCV Id: RCV001253760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Leu411Ser
CA415086584
NM_005629.4:c.1232T>C