Canonical Allele Identifier: PA658669751
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 479081
ClinVar RCV Id: RCV000561373 RCV000685483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1963Gly
CA382548540
NM_000051.4:c.5888A>G