Canonical Allele Identifier: PA645500523
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 232749
ClinVar RCV Id: RCV000218582 RCV000627918 RCV001762493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Gln654Pro
CA10579034
NM_000051.4:c.1961A>C