Canonical Allele Identifier: PA2827615989
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 378574
ClinVar RCV Id: RCV000440159 RCV001861495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Thr8Met
CA16605391
NM_001351527.2:c.23C>T