Canonical Allele Identifier: PA2826578327
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 990735
ClinVar RCV Id: RCV001278819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile3460Val
CA6910386
NM_001278055.2:c.10378A>G