Canonical Allele Identifier: PA2825034069
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1719891
ClinVar RCV Id: RCV002304056 RCV002346585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln1839Leu
CA382545777
NM_000051.4:c.5516A>T