Canonical Allele Identifier: PA2580390574
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1738588
ClinVar RCV Id: RCV002327799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Cys1398Phe
CA5297252
NM_015046.7:c.4193G>T