Canonical Allele Identifier: PA2826576644
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2890109
ClinVar RCV Id: RCV003750549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Thr1070Arg
CA6911492
NM_001278055.2:c.3209C>G