Canonical Allele Identifier: PA916034558
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 236781
ClinVar RCV Id: RCV000227613 RCV003362733
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro2648Thr
CA10582858
NM_001351834.2:c.7942C>A