Canonical Allele Identifier: PA2826577427
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1160698
ClinVar RCV Id: RCV001504896 RCV004037840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Glu2203Gly
CA6910975
NM_001278055.2:c.6608A>G