Canonical Allele Identifier: PA2573259339
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1389697
ClinVar RCV Id: RCV001898024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Arg3224Pro
CA6910583
NM_014363.6:c.9671G>C