Canonical Allele Identifier: PA915973008
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 810453
ClinVar RCV Id: RCV000999254 RCV002550734
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Pro1464Ser
CA5297209
NM_015046.7:c.4390C>T