Canonical Allele Identifier: PA1139729608
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 951351
ClinVar RCV Id: RCV001223243 RCV002411825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2599Ile
CA382561252
NM_001351834.2:c.7796C>T