Canonical Allele Identifier: PA2826578359
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2720928
ClinVar RCV Id: RCV003590834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Pro3509Thr
CA6910362
NM_001278055.2:c.10525C>A