Canonical Allele Identifier: PA2827617697
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 536384
ClinVar RCV Id: RCV000644823 RCV004533373 RCV004025671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Ser802Gly
CA375336078
NM_001351528.2:c.2404A>G