Canonical Allele Identifier: PA2827618049
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 579898
ClinVar RCV Id: RCV000703290 RCV003140115
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Ile1457Val
CA5297214
NM_001351528.2:c.4369A>G