Canonical Allele Identifier: PA2827616714
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2940290
ClinVar RCV Id: RCV003797648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Asp1443Asn
CA200807109
NM_001351527.2:c.4327G>A