Canonical Allele Identifier: PA2573203099
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1409818
ClinVar RCV Id: RCV001916071 RCV004042855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1851Pro
CA382545993
NM_001351834.2:c.5552T>C