Canonical Allele Identifier: PA658831569
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 558130
ClinVar RCV Id: RCV000674356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asp2157del
CA658823527
NM_014363.6:c.6469_6471del