Canonical Allele Identifier: PA2827618005
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 468505
ClinVar RCV Id: RCV000549234 RCV001167927 RCV001167928 RCV001288399 RCV002323994 RCV004541717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Ser1366Pro
CA5297271
NM_001351528.2:c.4096T>C