Canonical Allele Identifier: PA2580390547
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1923287
ClinVar RCV Id: RCV002604514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Ser1330Phe
CA200807584
NM_015046.7:c.3989C>T