Canonical Allele Identifier: PA2826577279
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1945689
ClinVar RCV Id: RCV002667312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp1991Val
CA6911085
NM_001278055.2:c.5972A>T