Canonical Allele Identifier: PA916034515
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Glu2621Gln
CA382561392
NM_001351834.2:c.7861G>C