Canonical Allele Identifier: PA2573204447
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1383065
ClinVar RCV Id: RCV001924496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu721Arg
CA382538769
NM_001351834.2:c.2162T>G