Canonical Allele Identifier: PA1139729959
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 922596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2668Lys
CA382561799
NM_001351834.2:c.8002G>A