Canonical Allele Identifier: PA2741945522
Gene: SACS HGNC NCBI

Linked Data

ClinVar Variation Id: 2913932
ClinVar RCV Id: RCV003751473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055178.3:p.Met4558Val
CA387504739
NM_014363.6:c.13672A>G