Canonical Allele Identifier: PA2827617671
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 536375
ClinVar RCV Id: RCV000644812 RCV002473087 RCV003233770 RCV003233769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Thr752Ala
CA5297637
NM_001351528.2:c.2254A>G