Canonical Allele Identifier: PA2827617796
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 440267
ClinVar RCV Id: RCV000507293 RCV000552319 RCV001089104 RCV002438234 RCV004541589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Asn1004Asp
CA5297500
NM_001351528.2:c.3010A>G