Canonical Allele Identifier: PA2826577648
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 882184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Pro2516Leu
CA6910840
NM_001278055.2:c.7547C>T