Canonical Allele Identifier: PA2827616664
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1992230
ClinVar RCV Id: RCV002795854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Thr1344Ser
CA375327519
NM_001351527.2:c.4031C>G
CA375327525
NM_001351527.2:c.4030A>T