Canonical Allele Identifier: PA2826577828
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2185805
ClinVar RCV Id: RCV002596331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Tyr2786His
CA6910716
NM_001278055.2:c.8356T>C