Canonical Allele Identifier: PA2827616654
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2684368
ClinVar RCV Id: RCV003482864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Lys1325Arg
CA375327766
NM_001351527.2:c.3974A>G