Canonical Allele Identifier: PA2827615989
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 378574

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Thr8Met
CA16605391
NM_001351527.2:c.23C>T