Canonical Allele Identifier: PA2580334342
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2138757
ClinVar RCV Id: RCV003050667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Lys4Arg
CA415075865
NM_005629.4:c.11A>G