Canonical Allele Identifier: PA2826576486
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 311553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile783Val
CA10639237
NM_001278055.2:c.2347A>G