Canonical Allele Identifier: PA2580203326
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1932979
ClinVar RCV Id: RCV002635686
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg692Gly
CA382537538
NM_001351834.2:c.2074C>G