Canonical Allele Identifier: PA096934
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2290
ClinVar RCV Id: RCV000002380 RCV000414273 RCV000789614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Thr3Ile
CA252185
NM_015046.7:c.8C>T