Canonical Allele Identifier: PA2573259349
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1405855
ClinVar RCV Id: RCV001906740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ser3317Gly
CA6910533
NM_014363.6:c.9949A>G