Canonical Allele Identifier: PA2826579018
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 938190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ala4418Asp
CA6909932
NM_001278055.2:c.13253C>A