Canonical Allele Identifier: PA2827616695
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Thr1402Ser
CA5297247
NM_001351527.2:c.4204A>T
CA375326975
NM_001351527.2:c.4205C>G