Canonical Allele Identifier: PA2826578816
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 699710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Pro4130Ser
CA6910073
NM_001278055.2:c.12388C>T