Canonical Allele Identifier: PA658664619
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 451915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Asp2162Gly
CA6911075
NM_014363.6:c.6485A>G