Canonical Allele Identifier: PA2741867146
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2887636
ClinVar RCV Id: RCV003606694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1846Thr
CA382545905
NM_001351834.2:c.5537T>C