Canonical Allele Identifier: PA2826578778
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2986893
ClinVar RCV Id: RCV003846548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile4082Thr
CA387507135
NM_001278055.2:c.12245T>C