Canonical Allele Identifier: PA2826578384
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2194663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Pro3542Leu
CA6910343
NM_001278055.2:c.10625C>T