Canonical Allele Identifier: PA2499244789
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1001433
ClinVar RCV Id: RCV001297736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Ile963Thr
CA387535835
NM_001278055.2:c.2888T>C