Canonical Allele Identifier: PA104610
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 11700
ClinVar RCV Id: RCV001508970 RCV000012466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Gly87Arg
CA256012
NM_005629.4:c.259G>A
CA415077143
NM_005629.4:c.259G>C