Canonical Allele Identifier: PA2826576158
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 448194

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Thr360Ala
CA6911906
NM_001278055.2:c.1078A>G