Canonical Allele Identifier: PA913191569
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 630859
ClinVar RCV Id: RCV000776869 RCV001856137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His683Tyr
CA382537433
NM_000051.4:c.2047C>T