Canonical Allele Identifier: PA2826577178
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1143578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Val1844Ile
CA6911161
NM_001278055.2:c.5530G>A