Canonical Allele Identifier: PA2826577846
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2167730
ClinVar RCV Id: RCV003086596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.His2803Pro
CA387515734
NM_001278055.2:c.8408A>C