Canonical Allele Identifier: PA2741867140
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2774686
ClinVar RCV Id: RCV003585876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys1834Arg
CA6265722
NM_001351834.2:c.5501A>G