Canonical Allele Identifier: PA2827617812
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 285878
ClinVar RCV Id: RCV000321789 RCV001222571 RCV002519195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Ser1019Tyr
CA5297486
NM_001351528.2:c.3056C>A