Canonical Allele Identifier: PA2826577729
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 448223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Gly2625Ala
CA6910788
NM_001278055.2:c.7874G>C