Canonical Allele Identifier: PA2826577172
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 555767
ClinVar RCV Id: RCV000671647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser1833del
CA658823552
NM_001278055.2:c.5496_5498del