Canonical Allele Identifier: PA2827616705
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 994756
ClinVar RCV Id: RCV001288402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Ile1424Val
CA5297231
NM_001351527.2:c.4270A>G