Canonical Allele Identifier: PA2826578398
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1806973
ClinVar RCV Id: RCV002474402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Pro3566Thr
CA387510655
NM_001278055.2:c.10696C>A