Canonical Allele Identifier: PA2826577292
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 558130
ClinVar RCV Id: RCV000674356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp2010del
CA658823527
NM_001278055.2:c.6028_6030del