Canonical Allele Identifier: PA2825852747
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 523485
ClinVar RCV Id: RCV000626885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136278.1:p.Ala288Val
CA415086472
NM_001142806.1:c.863C>T