Canonical Allele Identifier: PA2826576596
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 968494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Lys1001Thr
CA6911520
NM_001278055.2:c.3002A>C