Canonical Allele Identifier: PA2580203342
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2005257
ClinVar RCV Id: RCV002828484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met732Thr
CA382538947
NM_001351834.2:c.2195T>C