Canonical Allele Identifier: PA2827618023
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 994754
ClinVar RCV Id: RCV001288400 RCV003246833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Gly1401Val
CA5297248
NM_001351528.2:c.4202G>T