Canonical Allele Identifier: PA2827618035
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 155746
ClinVar RCV Id: RCV000143817 RCV000790205 RCV001049421 RCV000988269 RCV002326849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Lys1425Glu
CA233102
NM_001351528.2:c.4273A>G