Canonical Allele Identifier: PA2826578072
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 883268
ClinVar RCV Id: RCV001113531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp3113Gly
CA387513668
NM_001278055.2:c.9338A>G