Canonical Allele Identifier: PA658662191
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 468491
ClinVar RCV Id: RCV000526691 RCV002448727 RCV003480678 RCV004541714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Ser761Leu
CA5297629
NM_015046.7:c.2282C>T