Canonical Allele Identifier: PA2826577451
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 880850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg2236Cys
CA6910966
NM_001278055.2:c.6706C>T