Canonical Allele Identifier: PA2826578358
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 411693
ClinVar RCV Id: RCV000466695 RCV001288373 RCV001833594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Pro3505Thr
CA6910364
NM_001278055.2:c.10513C>A