Canonical Allele Identifier: PA2499250964
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1000731
ClinVar RCV Id: RCV001296900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2223Leu
CA382554857
NM_001351834.2:c.6667A>C