Canonical Allele Identifier: PA2827616101
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365374
ClinVar RCV Id: RCV000289058 RCV000346458 RCV001861345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Tyr237Cys
CA5297977
NM_001351527.2:c.710A>G