Canonical Allele Identifier: PA2826577151
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 528004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.His1806Leu
CA387524514
NM_001278055.2:c.5417A>T