Canonical Allele Identifier: PA2826578774
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2179813
ClinVar RCV Id: RCV002615240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Gln4079Leu
CA6910111
NM_001278055.2:c.12236A>T