Canonical Allele Identifier: PA891856121
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 569203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Arg3184His
CA6910605
NM_014363.6:c.9551G>A