Canonical Allele Identifier: PA2825035016
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2453926
ClinVar RCV Id: RCV003188061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ile2260Arg
CA382555456
NM_000051.4:c.6779T>G