Canonical Allele Identifier: PA2827615983
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 493501
ClinVar RCV Id: RCV000585415 RCV001860113 RCV002341496 RCV004530634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Ser2Gly
CA5298157
NM_001351527.2:c.4A>G