Canonical Allele Identifier: PA2826577907
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 863940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Tyr2896Cys
CA6910662
NM_001278055.2:c.8687A>G