Canonical Allele Identifier: PA2826577270
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1696314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp1981Gly
CA6911091
NM_001278055.2:c.5942A>G