Canonical Allele Identifier: PA2826577016
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1343991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ala1628Thr
CA246659263
NM_001278055.2:c.4882G>A