Canonical Allele Identifier: PA2580390535
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2142203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Tyr1297Phe
CA5297310
NM_015046.7:c.3890A>T