Canonical Allele Identifier: PA891852059
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 571505
ClinVar RCV Id: RCV000692670 RCV001830511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005620.1:p.Gly9Val
CA415075922
NM_005629.4:c.26G>T