Canonical Allele Identifier: PA916031943
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 187501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Leu615Pro
CA197807
NM_001351834.2:c.1844T>C