Canonical Allele Identifier: PA2827616656
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1923287
ClinVar RCV Id: RCV002604514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Ser1330Phe
CA200807584
NM_001351527.2:c.3989C>T