Canonical Allele Identifier: PA2580203845
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1735289
ClinVar RCV Id: RCV002364018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1275Thr
CA382524915
NM_001351834.2:c.3824T>C