Canonical Allele Identifier: PA2499250928
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1010644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2660del
CA1998811836
NM_001351834.2:c.7980_7982del