Canonical Allele Identifier: PA2580206764
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1762049
ClinVar RCV Id: RCV002419534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Cys2704Gly
CA382562132
NM_001351834.2:c.8110T>G