Canonical Allele Identifier: PA1139735464
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 927771
ClinVar RCV Id: RCV001191260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser865Gly
CA382544040
NM_001351834.2:c.2593A>G