Canonical Allele Identifier: PA2825036037
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 944244
ClinVar RCV Id: RCV001214602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln2714Arg
CA382562238
NM_000051.4:c.8141A>G