Canonical Allele Identifier: PA2573246074
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1556759
ClinVar RCV Id: RCV002202373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Phe439Val
CA10549490
NM_005629.4:c.1315T>G