Canonical Allele Identifier: PA891848279
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 579898
ClinVar RCV Id: RCV000703290 RCV003140115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Ile1457Val
CA5297214
NM_015046.7:c.4369A>G