Canonical Allele Identifier: PA2826577419
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2146373
ClinVar RCV Id: RCV003074528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp2192Gly
CA6910979
NM_001278055.2:c.6575A>G