Canonical Allele Identifier: PA2826577255
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2161923
ClinVar RCV Id: RCV003078817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Val1947Asp
CA387523501
NM_001278055.2:c.5840T>A