Canonical Allele Identifier: PA2826577540
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1209831
ClinVar RCV Id: RCV001579249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Tyr2336Cys
CA387519110
NM_001278055.2:c.7007A>G