Canonical Allele Identifier: PA1139728097
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 994757
ClinVar RCV Id: RCV001288403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Pro1438Ser
CA5297225
NM_015046.7:c.4312C>T