Canonical Allele Identifier: PA916008730
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 448203

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asn991Ser
CA387535393
NM_001278055.2:c.2972A>G