Canonical Allele Identifier: PA2580390151
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1944839
ClinVar RCV Id: RCV002639973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Met382Ile
CA375345424
NM_015046.7:c.1146G>T
CA375345426
NM_015046.7:c.1146G>C
CA375345427
NM_015046.7:c.1146G>A