Canonical Allele Identifier: PA916034384
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2508Arg
CA197186
NM_001351834.2:c.7522G>A
CA382560645
NM_001351834.2:c.7522G>C