Canonical Allele Identifier: PA2827617502
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1299688
ClinVar RCV Id: RCV002221638
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Met386Val
CA375345384
NM_001351528.2:c.1156A>G