Canonical Allele Identifier: PA2827616645
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1440642
ClinVar RCV Id: RCV001967718 RCV003136348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338456.1:p.Arg1311Cys
CA5297304
NM_001351527.2:c.3931C>T