Canonical Allele Identifier: PA1139731932
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 884013
ClinVar RCV Id: RCV001114844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ser3505Pro
CA387512044
NM_014363.6:c.10513T>C