Canonical Allele Identifier: PA2826577185
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 557488
ClinVar RCV Id: RCV000673637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Lys1853del
CA658823549
NM_001278055.2:c.5558_5560del