Canonical Allele Identifier: PA2741944032
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2926433
ClinVar RCV Id: RCV003786719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Val1451Glu
CA375326443
NM_015046.7:c.4352T>A