Canonical Allele Identifier: PA2573202878
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1434321
ClinVar RCV Id: RCV001984606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile1681Arg
CA382540374
NM_001351834.2:c.5042T>G