Canonical Allele Identifier: PA2826576636
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2038777
ClinVar RCV Id: RCV002895208
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.His1059Arg
CA6911498
NM_001278055.2:c.3176A>G