Canonical Allele Identifier: PA2580205689
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 2057744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Thr2228Ile
CA382554889
NM_001351834.2:c.6683C>T