Canonical Allele Identifier: PA658669534
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482579
ClinVar RCV Id: RCV000570105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asp1790Glu
CA382543419
NM_000051.4:c.5370T>A
CA382543424
NM_000051.4:c.5370T>G