Canonical Allele Identifier: PA2827616220
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 155742
ClinVar RCV Id: RCV000143813 RCV000626102 RCV000790203 RCV000791025 RCV001523409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Arg502Trp
CA233090
NM_001351527.2:c.1504C>T