Canonical Allele Identifier: PA2826578256
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 884011
ClinVar RCV Id: RCV001114842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Glu3365Gln
CA387511998
NM_001278055.2:c.10093G>C