Canonical Allele Identifier: PA2827616732
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 468508
ClinVar RCV Id: RCV000525003 RCV003243185 RCV003482284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Ala1479Val
CA5297200
NM_001351527.2:c.4436C>T