Canonical Allele Identifier: PA1139735674
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 845319
ClinVar RCV Id: RCV001048361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ile923Met
CA382545511
NM_001351834.2:c.2769T>G