Canonical Allele Identifier: PA2826579010
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2631109
ClinVar RCV Id: RCV003405847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ser4407Thr
CA387504764
NM_001278055.2:c.13219T>A