Canonical Allele Identifier: PA2573203926
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1500225

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2391Thr
CA382559554
NM_001351834.2:c.7171G>A