Canonical Allele Identifier: PA2826577435
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2081803
ClinVar RCV Id: RCV002995629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser2213Tyr
CA387520091
NM_001278055.2:c.6638C>A