Canonical Allele Identifier: PA2825035078
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1755814
ClinVar RCV Id: RCV002362131
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Cys2286Arg
CA382556697
NM_000051.4:c.6856T>C