Canonical Allele Identifier: PA2827618036
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1026940
ClinVar RCV Id: RCV001327470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.His1428Arg
CA5297230
NM_001351528.2:c.4283A>G