Canonical Allele Identifier: PA2827618053
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 810453
ClinVar RCV Id: RCV000999254 RCV002550734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Pro1464Ser
CA5297209
NM_001351528.2:c.4390C>T