Canonical Allele Identifier: PA2826577249
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2883001
ClinVar RCV Id: RCV003750437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asp1939Asn
CA6911110
NM_001278055.2:c.5815G>A