Canonical Allele Identifier: PA2826578400
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1979182
ClinVar RCV Id: RCV002742037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser3568Gly
CA246651687
NM_001278055.2:c.10702A>G