Canonical Allele Identifier: PA2826578735
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 946482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Thr4020Ile
CA6910139
NM_001278055.2:c.12059C>T