Canonical Allele Identifier: PA2573203776
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1468763
ClinVar RCV Id: RCV001970735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile2233Thr
CA382554927
NM_001351834.2:c.6698T>C