Canonical Allele Identifier: PA2827617741
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365364
ClinVar RCV Id: RCV000280363 RCV000372562 RCV000644850 RCV000789558 RCV001079301 RCV001848726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Val891Ala
CA5297553
NM_001351528.2:c.2672T>C