Canonical Allele Identifier: PA2825032078
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3018735
ClinVar RCV Id: RCV003879382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His943Arg
CA382545814
NM_000051.4:c.2828A>G