Canonical Allele Identifier: PA2827616814
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365352
ClinVar RCV Id: RCV000323303 RCV000380301 RCV002524587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Pro1642Thr
CA5297106
NM_001351527.2:c.4924C>A