Canonical Allele Identifier: PA2827616639
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1736031
ClinVar RCV Id: RCV002357471 RCV004534055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Gln1301Arg
CA5297309
NM_001351527.2:c.3902A>G