Canonical Allele Identifier: PA2573202040
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1520531
ClinVar RCV Id: RCV002030817 RCV002352762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His1264Asn
CA382524602
NM_001351834.2:c.3790C>A