Canonical Allele Identifier: PA2826576212
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2082356
ClinVar RCV Id: RCV002979953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile418Val
CA6911867
NM_001278055.2:c.1252A>G