Canonical Allele Identifier: PA2827616667
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 468504
ClinVar RCV Id: RCV000536880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Gln1351Glu
CA5297277
NM_001351527.2:c.4051C>G