Canonical Allele Identifier: PA2580354484
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2040870
ClinVar RCV Id: RCV002912756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.His1769Arg
CA6911268
NM_014363.6:c.5306A>G