Canonical Allele Identifier: PA2827617970
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1736056
ClinVar RCV Id: RCV002357482 RCV003883808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Arg1302Leu
CA375328048
NM_001351528.2:c.3905G>T