Canonical Allele Identifier: PA2573203947
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1518401

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2421Arg
CA382559747
NM_001351834.2:c.7262A>G