Canonical Allele Identifier: PA2825852728
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1321489
ClinVar RCV Id: RCV001779581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Ile272Met
CA415086178
NM_001142806.1:c.816C>G