Canonical Allele Identifier: PA2826577980
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2809587
ClinVar RCV Id: RCV003751723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp2990Gly
CA387514504
NM_001278055.2:c.8969A>G