Canonical Allele Identifier: PA2826577931
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1806988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Cys2935Tyr
CA6910645
NM_001278055.2:c.8804G>A