Canonical Allele Identifier: PA2827629718
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 3232279
ClinVar RCV Id: RCV004520962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser681Leu
CA2825001781
NM_001351834.2:c.2041_2042delinsCT