Canonical Allele Identifier: PA916033821
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 420012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly2063Glu
CA16619209
NM_001351834.2:c.6188G>A