Canonical Allele Identifier: PA2825851984
Gene: SLC6A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1343168
ClinVar RCV Id: RCV001843769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136277.1:p.Gly44Cys
CA415076392
NM_001142805.2:c.130G>T