Canonical Allele Identifier: PA2826577100
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2323109
ClinVar RCV Id: RCV002934137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Gly1734Ala
CA387525204
NM_001278055.2:c.5201G>C