Canonical Allele Identifier: PA1139731079
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 880850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Arg2383Cys
CA6910966
NM_014363.6:c.7147C>T