Canonical Allele Identifier: PA2741848785
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2727586
ClinVar RCV Id: RCV003588193
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264984.1:p.Asn920Ser
CA6911554
NM_001278055.2:c.2759A>G