Canonical Allele Identifier: PA2826579001
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1806958
ClinVar RCV Id: RCV002474387 RCV002571517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Arg4390Lys
CA6909938
NM_001278055.2:c.13169G>A