Canonical Allele Identifier: PA658662244
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 468504
ClinVar RCV Id: RCV000536880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Gln1351Glu
CA5297277
NM_015046.7:c.4051C>G