Canonical Allele Identifier: PA2573091292
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1311415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Pro1431Ala
CA5297229
NM_015046.7:c.4291C>G