Canonical Allele Identifier: PA2827616716
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1304958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Val1446Leu
CA375326482
NM_001351527.2:c.4336G>T
CA375326483
NM_001351527.2:c.4336G>C