Canonical Allele Identifier: PA094621
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 411693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Pro3652Thr
CA6910364
NM_014363.6:c.10954C>A