Canonical Allele Identifier: PA2827629924
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1001071
ClinVar RCV Id: RCV001297300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338764.1:p.Asp18Asn
CA382519232
NM_001351835.2:c.52G>A