Canonical Allele Identifier: PA658810462
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_055861.3:p.Glu385Lys
CA375345398
NM_015046.7:c.1153G>A