Canonical Allele Identifier: PA916034852
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142249
ClinVar RCV Id: RCV000131262 RCV000203831 RCV000589725 RCV001356460 RCV002265616 RCV002483265 RCV003474776
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2853Met
CA294334
NM_001351834.2:c.8558C>T