Canonical Allele Identifier: PA2827618032
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2943743
ClinVar RCV Id: RCV003803301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Glu1420Gly
CA375326768
NM_001351528.2:c.4259A>G