Canonical Allele Identifier: PA891856136
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 582271
ClinVar RCV Id: RCV000706307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Lys3319Glu
CA387513291
NM_014363.6:c.9955A>G