Canonical Allele Identifier: PA645437285
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 287041
ClinVar RCV Id: RCV000337874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Ala1490Gly
CA10605656
NM_014363.6:c.4469C>G