Canonical Allele Identifier: PA2827616665
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 448326

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Gln1349Glu
CA200807527
NM_001351527.2:c.4045C>G