Canonical Allele Identifier: PA2827616709
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1422645
ClinVar RCV Id: RCV001945664 RCV002331460 RCV003234140 RCV003234139 RCV003434358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Thr1433Ala
CA200807138
NM_001351527.2:c.4297A>G