Canonical Allele Identifier: PA2826576530
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2071683
ClinVar RCV Id: RCV002975773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile836Val
CA387537197
NM_001278055.2:c.2506A>G