Canonical Allele Identifier: PA2741943990
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 2929805
ClinVar RCV Id: RCV003784971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Arg1364del
CA590947259
NM_015046.7:c.4090_4092del
CA2579491637
NM_015046.7:c.4087_4089del