Canonical Allele Identifier: PA2826577458
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1209833
ClinVar RCV Id: RCV001579251

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Gly2243Asp
CA387519887
NM_001278055.2:c.6728G>A