Canonical Allele Identifier: PA645426488
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365341
ClinVar RCV Id: RCV000335520 RCV000399643 RCV001509370 RCV001861344 RCV002402087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Val2579Ile
CA5296343
NM_015046.7:c.7735G>A