Canonical Allele Identifier: PA2826576155
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2095365
ClinVar RCV Id: RCV003013772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ala357Thr
CA387548059
NM_001278055.2:c.1069G>A