Canonical Allele Identifier: PA658662247
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 448328
ClinVar RCV Id: RCV000517431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Ala1406Gly
CA200807227
NM_015046.7:c.4217C>G