Canonical Allele Identifier: PA2826576089
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Leu260Ile
CA6911950
NM_001278055.2:c.778C>A