Canonical Allele Identifier: PA1139735470
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 845539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu871Gly
CA382544185
NM_001351834.2:c.2612A>G