Canonical Allele Identifier: PA2826578230
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1929660
ClinVar RCV Id: RCV002626401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile3338Thr
CA6910449
NM_001278055.2:c.10013T>C