Canonical Allele Identifier: PA2826577963
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2085420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg2973His
CA6910632
NM_001278055.2:c.8918G>A