Canonical Allele Identifier: PA916034494
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 481211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Ala2602Thr
CA382561267
NM_001351834.2:c.7804G>A