Canonical Allele Identifier: PA2826578014
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 569203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg3037His
CA6910605
NM_001278055.2:c.9110G>A