Canonical Allele Identifier: PA2827617708
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 468493
ClinVar RCV Id: RCV000527749 RCV002456163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Thr816Ala
CA5297590
NM_001351528.2:c.2446A>G