Canonical Allele Identifier: PA2826577505
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1312308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile2289Val
CA387519591
NM_001278055.2:c.6865A>G