Canonical Allele Identifier: PA2580354911
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 1806973
ClinVar RCV Id: RCV002474402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Pro3713Thr
CA387510655
NM_014363.6:c.11137C>A