Canonical Allele Identifier: PA2573203878
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1513356
ClinVar RCV Id: RCV002026129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu2345Ser
CA382558859
NM_001351834.2:c.7034T>C