Canonical Allele Identifier: PA2826576540
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 281206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile852Thr
CA6911580
NM_001278055.2:c.2555T>C