Canonical Allele Identifier: PA2826576108
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 848646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ala286Pro
CA6911933
NM_001278055.2:c.856G>C