Canonical Allele Identifier: PA645426494
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365337
ClinVar RCV Id: RCV000299852 RCV000359404 RCV001662350 RCV003372694 RCV003766099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Pro2625Leu
CA5296299
NM_015046.7:c.7874C>T