Canonical Allele Identifier: PA2827616681
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 448327
ClinVar RCV Id: RCV000516516 RCV002527524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Lys1374Glu
CA5297266
NM_001351527.2:c.4120A>G