Canonical Allele Identifier: PA2499271539
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040216
ClinVar RCV Id: RCV001343819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Ala399Val
CA415086399
NM_005629.4:c.1196C>T