Canonical Allele Identifier: PA2826576739
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311545

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ala1226Pro
CA6911431
NM_001278055.2:c.3676G>C