Canonical Allele Identifier: PA2826577012
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2304978
ClinVar RCV Id: RCV002874355

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Val1623Gly
CA246659289
NM_001278055.2:c.4868T>G