Canonical Allele Identifier: PA2826577824
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1140538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg2785Trp
CA6910719
NM_001278055.2:c.8353C>T