Canonical Allele Identifier: PA2827617971
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2614391
ClinVar RCV Id: RCV003364829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Arg1302Trp
CA5297308
NM_001351528.2:c.3904C>T