Canonical Allele Identifier: PA2827617505
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1341357
ClinVar RCV Id: RCV001829275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Leu389del
CA2573053118
NM_001351528.2:c.1165_1167del