Canonical Allele Identifier: PA2826577158
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1952121
ClinVar RCV Id: RCV002695207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp1819Asn
CA6911178
NM_001278055.2:c.5455G>A