Canonical Allele Identifier: PA2827616065
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 536403
ClinVar RCV Id: RCV000644846 RCV001167587 RCV001167588 RCV001288404 RCV004025672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Asn144Ser
CA5298042
NM_001351527.2:c.431A>G