Canonical Allele Identifier: PA658664718
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 448191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile4347Val
CA6910031
NM_014363.6:c.13039A>G