Canonical Allele Identifier: PA2827616715
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1371290
ClinVar RCV Id: RCV001899548
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Val1445Ala
CA5297220
NM_001351527.2:c.4334T>C