Canonical Allele Identifier: PA916034102
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2287Arg
CA382556715
NM_001351834.2:c.6859G>A
CA382556716
NM_001351834.2:c.6859G>C