Canonical Allele Identifier: PA645503398
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233040
ClinVar RCV Id: RCV000222419 RCV000812354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly1925Glu
CA6265784
NM_000051.4:c.5774G>A