Canonical Allele Identifier: PA2827617634
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 365368
ClinVar RCV Id: RCV000344541 RCV000390382 RCV000803584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338457.1:p.Asn668Ser
CA5297681
NM_001351528.2:c.2003A>G