Canonical Allele Identifier: PA891856022
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 572396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.His1969Arg
CA6911173
NM_014363.6:c.5906A>G