Canonical Allele Identifier: PA2827616701
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 155745
ClinVar RCV Id: RCV000143816 RCV000790204 RCV000988270 RCV001002069 RCV001041860 RCV002326848 RCV001167322 RCV004532621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Asn1409Tyr
CA233099
NM_001351527.2:c.4225A>T