Canonical Allele Identifier: PA2826577417
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2195776
ClinVar RCV Id: RCV002628936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Met2188Val
CA6910982
NM_001278055.2:c.6562A>G