Canonical Allele Identifier: PA2827618042
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2930098
ClinVar RCV Id: RCV003787456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Cys1442Tyr
CA375326521
NM_001351528.2:c.4325G>A