Canonical Allele Identifier: PA2499251062
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1040289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Met1909Thr
CA6265763
NM_001351834.2:c.5726T>C