Canonical Allele Identifier: PA658698970
Gene: SETX HGNC NCBI

Linked Data

ClinVar Variation Id: 493499
ClinVar RCV Id: RCV000585562 RCV001860112 RCV003233754 RCV003233755 RCV004530633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055861.3:p.Leu2473Val
CA5296396
NM_015046.7:c.7417C>G