Canonical Allele Identifier: PA2499251056
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1054109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys1807Glu
CA382543911
NM_001351834.2:c.5419A>G