Canonical Allele Identifier: PA2580203908
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1999729
ClinVar RCV Id: RCV002819812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val1345Ala
CA382527733
NM_001351834.2:c.4034T>C