Canonical Allele Identifier: PA2826576355
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2075406
ClinVar RCV Id: RCV002967703

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile600Thr
CA246663735
NM_001278055.2:c.1799T>C