Canonical Allele Identifier: PA916034923
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 186276

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2904Gly
CA194327
NM_001351834.2:c.8711A>G