Canonical Allele Identifier: PA2826576602
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2190097
ClinVar RCV Id: RCV002636974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Lys1008Thr
CA6911517
NM_001278055.2:c.3023A>C