Canonical Allele Identifier: PA2826578214
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1176616
ClinVar RCV Id: RCV001532229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.His3311Tyr
CA387512359
NM_001278055.2:c.9931C>T