Canonical Allele Identifier: PA915973139
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 807687
ClinVar RCV Id: RCV000995873 RCV001093196 RCV001095488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Ile1942Thr
CA5296889
NM_015046.7:c.5825T>C