Canonical Allele Identifier: PA2826578119
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1405855
ClinVar RCV Id: RCV001906740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser3170Gly
CA6910533
NM_001278055.2:c.9508A>G