Canonical Allele Identifier: PA658662204
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 468495
ClinVar RCV Id: RCV000552679 RCV001165886 RCV001165887 RCV002431641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Ser906Leu
CA5297546
NM_015046.7:c.2717C>T