Canonical Allele Identifier: PA2826577911
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1409237
ClinVar RCV Id: RCV001913536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg2901His
CA6910659
NM_001278055.2:c.8702G>A