Canonical Allele Identifier: PA2827616172
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 536386
ClinVar RCV Id: RCV000644825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Glu385Lys
CA375345398
NM_001351527.2:c.1153G>A