Canonical Allele Identifier: PA115942
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 802789
ClinVar RCV Id: RCV000988729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Ala2626Pro
CA115940
NM_000051.4:c.7876G>C