Canonical Allele Identifier: PA658671262
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 449186
ClinVar RCV Id: RCV000523929 RCV001300034 RCV001834680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Arg391Gln
CA10549445
NM_005629.4:c.1172G>A