Canonical Allele Identifier: PA2826577019
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2149958

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser1632Leu
CA6911264
NM_001278055.2:c.4895C>T