Canonical Allele Identifier: PA2827617989
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2590109
ClinVar RCV Id: RCV003363663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Asn1339del
CA1129644155
NM_001351528.2:c.4017_4019del