Canonical Allele Identifier: PA2580203698
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2428823
ClinVar RCV Id: RCV003120424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Arg1106Thr
CA382517470
NM_001351834.2:c.3317G>C