Canonical Allele Identifier: PA2826578769
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 235607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asn4070Asp
CA6910119
NM_001278055.2:c.12208A>G