Canonical Allele Identifier: PA2826576807
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 212114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asn1342Ser
CA207202
NM_001278055.2:c.4025A>G