Canonical Allele Identifier: PA2827618050
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 1943382
ClinVar RCV Id: RCV002670844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Val1458Ala
CA375326399
NM_001351528.2:c.4373T>C