Canonical Allele Identifier: PA2827616708
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1311415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Pro1431Ala
CA5297229
NM_001351527.2:c.4291C>G