Canonical Allele Identifier: PA2826577750
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2172201
ClinVar RCV Id: RCV003090498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Lys2648Arg
CA387516757
NM_001278055.2:c.7943A>G