Canonical Allele Identifier: PA891856188
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 576933
ClinVar RCV Id: RCV000699567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Arg4274Gly
CA387506853
NM_014363.6:c.12820A>G