Canonical Allele Identifier: PA2826577170
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1806965
ClinVar RCV Id: RCV002474394 RCV002571519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Phe1832Val
CA6911168
NM_001278055.2:c.5494T>G