Canonical Allele Identifier: PA2827616710
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 994757
ClinVar RCV Id: RCV001288403
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Pro1438Ser
CA5297225
NM_001351527.2:c.4312C>T