Canonical Allele Identifier: PA645426364
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365353
ClinVar RCV Id: RCV000348389 RCV000400900 RCV000644810 RCV002338959 RCV003482252 RCV004544710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Arg1538Trp
CA5297167
NM_015046.7:c.4612C>T