Canonical Allele Identifier: PA2826577418
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2138947
ClinVar RCV Id: RCV003050759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile2190Val
CA6910980
NM_001278055.2:c.6568A>G