Canonical Allele Identifier: PA2827617986
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1896044
ClinVar RCV Id: RCV002571845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Pro1331del
CA5297289
NM_001351528.2:c.3992_3994del