Canonical Allele Identifier: PA2573203149
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 1380210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.His1865Asn
CA228389817
NM_001351834.2:c.5593C>A