Canonical Allele Identifier: PA2826577607
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 448220
ClinVar RCV Id: RCV000517402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Leu2441His
CA387518295
NM_001278055.2:c.7322T>A