Canonical Allele Identifier: PA2573203246
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1472532
ClinVar RCV Id: RCV002005028 RCV002352681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Pro1922Thr
CA382548277
NM_001351834.2:c.5764C>A