Canonical Allele Identifier: PA2825852778
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2161659
ClinVar RCV Id: RCV003089607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Leu314Phe
CA415086729
NM_001142806.1:c.940C>T