Canonical Allele Identifier: PA2825035922
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1761622
ClinVar RCV Id: RCV002419195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2669Met
CA382561812
NM_000051.4:c.8007T>G