Canonical Allele Identifier: PA658669551
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 453580
ClinVar RCV Id: RCV000531799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gly1818Glu
CA658656257
NM_000051.4:c.5453_5454delinsAA