Canonical Allele Identifier: PA2580161496
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2290132
ClinVar RCV Id: RCV002854159 RCV003991050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Trp9Arg
CA415077941
NM_001142806.1:c.25T>A
CA415077944
NM_001142806.1:c.25T>C