Canonical Allele Identifier: PA2580355132
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2285514
ClinVar RCV Id: RCV002840791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Phe4432Ser
CA6909985
NM_014363.6:c.13295T>C