Canonical Allele Identifier: PA2826577428
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2082858

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asn2204Ser
CA387520154
NM_001278055.2:c.6611A>G