Canonical Allele Identifier: PA2499250877
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1016582
ClinVar RCV Id: RCV001315605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln298Pro
CA382529622
NM_001351834.2:c.893A>C