Canonical Allele Identifier: PA2826578035
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2417044
ClinVar RCV Id: RCV003111872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser3066Gly
CA6910592
NM_001278055.2:c.9196A>G