Canonical Allele Identifier: PA916033628
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 233040

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly1925Glu
CA6265784
NM_001351834.2:c.5774G>A