Canonical Allele Identifier: PA2826577191
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2085224
ClinVar RCV Id: RCV002996165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Val1857Ala
CA6911150
NM_001278055.2:c.5570T>C