Canonical Allele Identifier: PA658670097
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 482702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Lys2302Arg
CA382556982
NM_000051.4:c.6905A>G