Canonical Allele Identifier: PA2826577413
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2079669
ClinVar RCV Id: RCV002998699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile2185Val
CA6910985
NM_001278055.2:c.6553A>G