Canonical Allele Identifier: PA916034267
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2422Lys
CA382559752
NM_001351834.2:c.7264G>A