Canonical Allele Identifier: PA916033516
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 407588
ClinVar RCV Id: RCV000476188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu1842Arg
CA16613160
NM_001351834.2:c.5525T>G