Canonical Allele Identifier: PA2829763934
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1001433
ClinVar RCV Id: RCV001297736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile1110Thr
CA387535835
NM_014363.6:c.3329T>C