Canonical Allele Identifier: PA2580203299
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1783693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys659Glu
CA382536852
NM_001351834.2:c.1975A>G