Canonical Allele Identifier: PA1139728037
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 994754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Gly1401Val
CA5297248
NM_015046.7:c.4202G>T