Canonical Allele Identifier: PA2827616711
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 805417
ClinVar RCV Id: RCV000992938 RCV001038162 RCV003233893 RCV003233894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Leu1439Ser
CA375326558
NM_001351527.2:c.4316T>C