Canonical Allele Identifier: PA2826576926
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Leu1499Met
CA6911320
NM_001278055.2:c.4495C>A