Canonical Allele Identifier: PA645426491
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365339
ClinVar RCV Id: RCV000328640 RCV000383186 RCV000699627 RCV000999251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Arg2605Gln
CA5296314
NM_015046.7:c.7814G>A