Canonical Allele Identifier: PA2826578392
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 938832
ClinVar RCV Id: RCV001208129 RCV001828667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile3559Val
CA6910338
NM_001278055.2:c.10675A>G