Canonical Allele Identifier: PA645437579
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 411694
ClinVar RCV Id: RCV000473308 RCV000594324 RCV000765121 RCV001848817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ile2749Val
CA6910801
NM_014363.6:c.8245A>G