Canonical Allele Identifier: PA658669609
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453588
ClinVar RCV Id: RCV000541198 RCV000777200
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Thr1864Arg
CA382546184
NM_000051.4:c.5591C>G