Canonical Allele Identifier: PA2827618027
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1738767
ClinVar RCV Id: RCV002327978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Leu1405Phe
CA5297246
NM_001351528.2:c.4213C>T