Canonical Allele Identifier: PA2827618021
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1738588
ClinVar RCV Id: RCV002327799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Cys1398Phe
CA5297252
NM_001351528.2:c.4193G>T