Canonical Allele Identifier: PA2580354639
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2147973
ClinVar RCV Id: RCV003068617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Glu2442Gly
CA6910929
NM_014363.6:c.7325A>G