Canonical Allele Identifier: PA916034538
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 220528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Asp2634Glu
CA348440
NM_001351834.2:c.7902T>G
CA382561479
NM_001351834.2:c.7902T>A