Canonical Allele Identifier: PA2826578856
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2149722
ClinVar RCV Id: RCV003071687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg4178Gln
CA6910039
NM_001278055.2:c.12533G>A