Canonical Allele Identifier: PA2827616642
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2223724
ClinVar RCV Id: RCV002673510
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Arg1302Gln
CA375328045
NM_001351527.2:c.3905G>A