Canonical Allele Identifier: PA2499251200
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1027190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Val2298Ile
CA382556891
NM_001351834.2:c.6892G>A