Canonical Allele Identifier: PA2825852735
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 465141
ClinVar RCV Id: RCV000551024 RCV000623839 RCV001572173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Arg276Trp
CA415086241
NM_001142806.1:c.826C>T