Canonical Allele Identifier: PA2825852050
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066432
ClinVar RCV Id: RCV003991436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Gly113Asp
CA415077715
NM_001142805.2:c.338G>A