Canonical Allele Identifier: PA2825033000
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 824542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.His1352Tyr
CA382527965
NM_000051.4:c.4054C>T