Canonical Allele Identifier: PA2580204746
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1719891

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln1839Leu
CA382545777
NM_001351834.2:c.5516A>T