Canonical Allele Identifier: PA2827617991
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 805415
ClinVar RCV Id: RCV000992936 RCV002354901 RCV001858762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Lys1341del
CA5297283
NM_001351528.2:c.4020_4022del