Canonical Allele Identifier: PA2826577433
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1922042
ClinVar RCV Id: RCV002613493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Glu2210Gly
CA6910973
NM_001278055.2:c.6629A>G