Canonical Allele Identifier: PA2573204209
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1351252
ClinVar RCV Id: RCV002044589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys2670Glu
CA382561814
NM_001351834.2:c.8008A>G