Canonical Allele Identifier: PA2826577006
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 554128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.His1622del
CA658823450
NM_001278055.2:c.4863_4865del