Canonical Allele Identifier: PA2826577571
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 964871
ClinVar RCV Id: RCV001239185
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile2385Thr
CA387518683
NM_001278055.2:c.7154T>C