Canonical Allele Identifier: PA916031973
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 573111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Lys640Glu
CA382536420
NM_001351834.2:c.1918A>G