Canonical Allele Identifier: PA2826577162
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 572396
ClinVar RCV Id: RCV000693766 RCV001825352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.His1822Arg
CA6911173
NM_001278055.2:c.5465A>G