Canonical Allele Identifier: PA2825030934
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 847882
ClinVar RCV Id: RCV001051519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile438Met
CA6264798
NM_000051.4:c.1314A>G