Canonical Allele Identifier: PA2826577849
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2237298
ClinVar RCV Id: RCV002723917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp2807Gly
CA387515706
NM_001278055.2:c.8420A>G