Canonical Allele Identifier: PA916033526
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 825813
ClinVar RCV Id: RCV001024244 RCV002298844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His1847Asp
CA382545915
NM_001351834.2:c.5539C>G