Canonical Allele Identifier: PA2826577488
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 805304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Phe2274Tyr
CA387519683
NM_001278055.2:c.6821T>A