Canonical Allele Identifier: PA2826577496
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2062222

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg2279Gln
CA6910937
NM_001278055.2:c.6836G>A