Canonical Allele Identifier: PA1139727374
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 848073
ClinVar RCV Id: RCV001051753 RCV002365696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ser2289Pro
CA382556745
NM_001351834.2:c.6865T>C