Canonical Allele Identifier: PA2826577154
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2892833
ClinVar RCV Id: RCV003750595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp1808Tyr
CA387524492
NM_001278055.2:c.5422G>T