Canonical Allele Identifier: PA2827616957
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 448338
ClinVar RCV Id: RCV000518592 RCV002525079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Asn1935Ser
CA5296892
NM_001351527.2:c.5804A>G