Canonical Allele Identifier: PA2827617069
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2286
ClinVar RCV Id: RCV000002376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Pro2213Leu
CA252178
NM_001351527.2:c.6638C>T