Canonical Allele Identifier: PA2827616644
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1736278
ClinVar RCV Id: RCV002357562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Arg1311His
CA5297303
NM_001351527.2:c.3932G>A